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Comparison of Surgery and Medicine on the Impact of Diverticulitis (COSMID) Trial

Offene Rekrutierung
Die Details der klinischen Studie sind hauptsächlich auf Englisch verfügbar. Trial Radar KI kann jedoch helfen! Klicken Sie einfach auf 'Studie erklären', um die Informationen zur Studie in der ausgewählten Sprache anzuzeigen und zu besprechen.
Die klinische Studie NCT04095663 (COSMID) ist eine interventionsstudie zur Untersuchung von Divertikulitis und hat den Status offene rekrutierung. Die Studie startete am 1. Oktober 2019 und soll 250 Teilnehmer aufnehmen. Durchgeführt von University of Washington ist der Abschluss für 1. Februar 2027 geplant. Die Daten von ClinicalTrials.gov wurden zuletzt am 13. November 2025 aktualisiert.
Kurzbeschreibung
The COSMID (Comparison of Surgery and Medicine on the Impact of Diverticulitis) trial is a pragmatic, patient-level randomized superiority trial of elective colectomy vs. best medical management for patients with quality of life (QoL) limiting diverticular disease. A parallel observational cohort will include those who are disinclined to have their treatment choice randomized, but are willing to contribute information about their outcomes. The goal of the COSMID trial is to answer the question: For patients with QoL-limiting diverticular disease, is elective colectomy more effective than best medical management? The hypothesis being tested in the COSMID trial is that patient-reported outcomes (PROs) among patients in the surgery arm will be superior to those in the best medical management arm.
Ausführliche Beschreibung
For over 50 years, professional society recommendations for the management of uncomplicated diverticulitis included early elective surgery to prevent the need for an emergency operation and avoid the risk of colostomy. Over the last 15 years the notion that a patient must have a certain number of episodes of acute uncomplicated diverticulitis (AUD) before undergoing elective colectomy has changed dramatically. This was, in part, due to studies showing that emergency surgery for complicated disease is much more likely to be needed during the first episode of diverticulitis, making the notion of prophylactic elective colectomy for AUD less relevant. Furthermore, clinicians realized that most recurrent episodes of AUD could be managed with outpatient antibiotics alone and that "best medical management" - including fiber supplementation, mesalazine, rifamycin and probiotics - could reduce symptoms between episodes of AUD. All of the components of best medical management have some, albeit limited, evidence of effectiveness, most in improving symptoms rather than reducing the risk of recurrence and are relatively safe and inexpensive. Best medical management is far less invasive than elective surgery but infrequently prescribed the US, in part because of limited insurance coverage. Alternatively, resection removes the diseased segment of colon, does relieve symptoms and decreases the risk of recurrence.

In 2014, guidelines from the American Society of Colorectal Surgeons (ASCRS) abandoned "episode count" as an indication for surgery in patients with AUD and instead recommended individualizing the decision to operate for AUD based on the "effects on lifestyle (professional and personal) of recurrent attacks". Decision making about surgery in patients with lingering symptoms after recovery from an episode of AUD has not been the specific focus of an ASCRS guideline, but recommendations about elective surgery emphasize individualizing decision making based on the overall impact of the disease on the patient.These recommendations for individualization of treatment based on the quality of life (QoL) impact of recurrent AUD and lingering symptoms highlight the decision that hundreds of thousands of people now have to make each year. Based on the effect of the disease on their QoL they must choose between two very different treatment options: elective colectomy vs. best medical management. While the recommendation to individualize treatment based on the QoL impact is a step forward in advancing patient-centered care, the comparative effectiveness of these two treatments on symptoms and QoL has not been well studied.

This will be a multi-site, open randomized trial in which participants with either recurrent AUD or lingering symptoms after an episode of AUD are randomized to one of two initial treatment strategies, elective segmental colectomy (performed laparoscopically when possible) and best medical management.

Offizieller Titel

Comparison of Surgery and Medicine on the Impact of Diverticulitis (COSMID) Trial

Erkrankungen
Divertikulitis
Weitere Studien-IDs
  • COSMID
  • STUDY00007409
NCT-Nummer
Studienbeginn (tatsächlich)
2019-10-01
Zuletzt aktualisiert
2025-11-13
Studienende (vorauss.)
2027-02-01
Geplante Rekrutierung
250
Studientyp
Interventionsstudie
PHASE
Nicht zutreffend
Status
Offene Rekrutierung
Primäres Ziel
Behandlung
Zuteilungsmethode
Randomisiert
Interventionsmodell
Parallel
Verblindung
Keine (offene Studie)
Studienarme/Interventionen
Teilnehmergruppe/StudienarmIntervention/Behandlung
Aktives VergleichspräparatPartial Colectomy
Elective segmental colectomy for diverticular disease involves removal of the segment of colon (most commonly sigmoid and/or left colon) where there has been disease identified by computed tomography imaging or colonoscopy. Elective colectomy usually removes the affected colon along with adjacent segments that have diverticula, with a primary anastomosis performed to reestablish bowel continuity. Most surgeons now perform the procedure using a laparoscopic approach, when possible, and sometimes use a temporary, protective stoma if the re-connection is considered high-risk. The technique for laparoscopic resection is not specified by the protocol (allows for any number of laparoscopic port sites, all incision types, hand-assistance and robotic) with details of the technique recorded. If randomized to elective colectomy, patients will be encouraged to undergo the procedure within 6 weeks of assignment.
Partial Colectomy
Most partial colectomies are performed using a laparoscopic approach, when possible, and surgeons sometimes use a temporary, protective stoma if the re-connection is considered high risk.
Aktives VergleichspräparatMedical Management
Medical management for diverticular disease has been used for over 30 years and includes a set of interventions, all components of which have been the subject of small, but often positive trials. All patients randomized to medical management or who select it as their treatment in the observational cohort will view a video (provided in English and Spanish) that explains each element of the medical management "toolbox": diet and exercise recommendations, fiber supplementation (e.g., augmenting dietary fiber or over the counter fiber supplements), with mesalazine tablets or suppositories, probiotics and rifamycin. In consultation with their physician, they will be recommended to a regimen of diet and exercise and fiber supplementation. Clinicians will be asked to consider rifamycin (dose/frequency) for those with AUD who are not responding to diet and exercise and mesalazine (dose/frequency) for those with lingering symptoms who are not responding to diet and exercise.
Medizinische Betreuung
Patients will be offered a varying combination of tools from the best medical management "toolbox" (diet and exercise, fiber supplementation/probiotics, and rifamycin/mesalazine) depending on what they have already tried. Based on the "evidence-based best medical toolbox" clinicians will be asked to consider rifamycin (dose/frequency) for those with AUD who are not responding to diet and exercise and mesalazine (dose/frequency) for those with lingering symptoms who are not responding to diet and exercise.
Hauptergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Patient-reported quality of life as measured by Gastrointestinal Quality of Life Index (GIQLI)
A 36-item questionnaire assessing 5 domains: GI symptoms, physical function, emotional well-being, social well-being, and perception of medical treatment measured by a single item question. Each item has 5 response choices (i.e., all of the time, most of the time, some of the time, a little of the time, never). In addition, the measure produces an overall quality of life score (0-144) where higher numbers indicate greater QoL.
Mean GIQLI at 6, 9, and 12 months following randomization to treatment
Nebenergebnismessungen
ErgebnismessungBeschreibung der MessungZeitrahmen
Diverticulitis Quality of Life (DV-QoL) instrument
A 17-item questionnaire including a pain scale and questions about about physical, emotional, and social effects of diverticulitis over the past 2 weeks, with a total score ranging from 0 (best) to 10 (worst) with higher scores reflecting worse quality of life effects from diverticulitis.
Baseline, 12 months, 24 months
Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health measure
A 10-item instrument measuring domains that can be scored into a Global Physical Health component and Global Mental Health component. Each item includes 5 response choices, with the exception of the common 11-point pain intensity item ("How would you rate your pain on average?" with 0=no pain and 10=worst imaginable pain), where higher scores reflect more severe symptoms/impairment.
Baseline; 6, 12, 24, 36 months
Decision Regret Scale
A 5-item validated questionnaire that measures regret among patients following a specific treatment decision. Scores range from 0-100 and higher scores reflect higher levels of regret. While developed for use in patients undergoing treatment for cancer, the questions are general in nature and adaptable to diverse clinical experiences.
6 and 36 months
Work Productivity and Activity Impairment instrument
A 6-item instrument used to measure the effect of general health and symptom severity on work productivity and regular activities during the past seven days. Scores are calculated applying algorithms to the five numerical responses, three of which are continuous variables (hours) and two of which are a scale from 0-10, then converting to a percentage, with higher WPAI scores indicating greater impairment and less productivity. The WPAI measures work productivity loss due to general health or a specified health problem. This questionnaire has been validated for use in many gastrointestinal diseases, including gastroesophageal reflux disease, irritable bowel syndrome, and Crohn's disease.
Baseline; 6, 12, 18, 24, 30, 36 months
Eignungskriterien

Zugelassene Altersgruppen
Erwachsene, Ältere Erwachsene
Mindestalter
18 Years
Zugelassene Geschlechter
Alle
  • Adults ≥18 years
  • At least one episode of diverticulitis confirmed by CT scan and a colonoscopy (completed or scheduled) to rule out or screen for other colon pathology in accordance with colorectal cancer screening guidelines
  • Persistent signs, symptoms, or concerns related to diverticulitis after recovery from an episode of left-sided diverticulitis
  • Self-reported QoL limitation (assessed with 12 questions modified from the Diverticulitis Quality of Life [DV-QOL] instrument).

  • Unable to consent in English or Spanish
  • Current diagnosis or previous endoscopic or surgical interventions for fistula, or stricture or current significant bleeding, related to diverticulitis
  • Last episode of acute diverticulitis currently unresolved (i.e., on antibiotics for diverticulitis; drain in place)
  • Previous operation for diverticulitis
  • Right-sided diverticulitis
  • Immunodeficiency (e.g., absolute neutrophil count <500/mm3, chronic immunosuppressive drugs like oral corticosteroids, anti-TNF agents, or known AIDS [i.e., recent CD4 count <200] assessed by patient history)
  • Actively undergoing chemotherapy or radiation for malignancy
  • Expectant or concurrent hemodialysis, peritoneal dialysis, treatments using indwelling venous catheters, or conditions putting patient at risk for bacterial seeding
  • Diagnosis of inflammatory bowel disease (i.e., Crohn's, ulcerative colitis)
  • Taking prescription medication for irritable bowel syndrome
  • Intolerance or allergy to all medications in the medical management arm
  • Surgeon is unwilling to offer surgery due to comorbid or prior surgical conditions that contraindicate elective surgery (e.g., liver failure, renal failure, malignancy, "frozen abdomen")
  • Abdominal/pelvic surgery within the past month
  • Pregnant or expecting to become pregnant in the 30 days following baseline/screening
  • Unable to consent to research or self-respond to follow-up surveys (e.g., altered mental status)
  • Currently incarcerated in a detention facility or in police custody at baseline/screening (patients wearing a monitoring device can be enrolled)
  • Prior enrollment in the COSMID study or planning on enrollment in another investigational drug or vaccine while on study treatment
  • Unable or unwilling to return, be contacted for, or complete research surveys.
Patient-Centered Outcomes Research Institute logoPatient-Centered Outcomes Research Institute
Verantwortliche Partei
David Flum, Hauptprüfer, Professor, School of Medicine: Surgery, University of Washington
Zentrale Studienkontakte
Kontakt: Kelsey M Pullar, MPH, 206 221-8247, [email protected]
Kontakt: Erin E Fannon, 206 685-9770, [email protected]
29 Studienstandorte in 1 Ländern

California

Cedars-Sinai Medical Center, Los Angeles, California, 90048, United States
Aktiv, nicht rekrutierend
UC San Diego Health, San Diego, California, 92103, United States
Aktiv, nicht rekrutierend
UCSF Health, San Francisco, California, 94143, United States
Jenny Broering, Kontakt, [email protected]
Offene Rekrutierung
Stanford University Medical Center, Stanford, California, 94305, United States
Kristen Davis, Kontakt, [email protected]
Offene Rekrutierung

Colorado

University of Colorado, Denver, Colorado, 80045, United States
Tracey MacDermott, Kontakt, [email protected]
Offene Rekrutierung

Florida

University of Florida, Gainesville, Florida, 32608, United States
Amber Bouton, Kontakt, [email protected]
Offene Rekrutierung
University of South Florida, Tampa, Florida, 33606, United States
Avennette Pinto, Kontakt, [email protected]
Offene Rekrutierung

Georgia

Memorial Health University Medical Center, Savannah, Georgia, 31404, United States
Anne Brooks, Kontakt, [email protected]
Offene Rekrutierung

Illinois

Rush University Medical Center, Chicago, Illinois, 60612, United States
Matthew Johnson, Kontakt, [email protected]
Offene Rekrutierung
Northwestern University, Evanston, Illinois, 60201, United States
Rose Arrieta, Kontakt, [email protected]
Offene Rekrutierung

Iowa

University of Iowa Healthcare, Iowa City, Iowa, 52242, United States
Jessica Danielson, Kontakt, [email protected]
Offene Rekrutierung

Massachusetts

Boston University Medical Center, Boston, Massachusetts, 02118, United States
Marina Malikova, Kontakt, [email protected]
Offene Rekrutierung
Lahey Clinic, Burlington, Massachusetts, 01805, United States
Kameron Ky, Kontakt, [email protected]
Offene Rekrutierung

New York

Albany Medical College, Albany, New York, 12208, United States
Aktiv, nicht rekrutierend
New York Presbyterian-Queens, Flushing, New York, 11355, United States
Susan Ingenito, Kontakt, [email protected]
Offene Rekrutierung
Columbia University Medical Center, New York, New York, 10027, United States
Ken Watanabe, Kontakt, [email protected]
Offene Rekrutierung
Weill Cornell Medicine, New York, New York, 10065, United States
Jordan Augsburger, Kontakt, [email protected]
Offene Rekrutierung
University of Rochester Medical Center, Rochester, New York, 14618, United States
I Marianetti, Kontakt, [email protected]
Offene Rekrutierung

North Carolina

Atrium Health-Carolinas Medical Center, Charlotte, North Carolina, 28203, United States
Colie Kaiser, Kontakt, [email protected]
Offene Rekrutierung

Ohio

Mount Carmel Health Systems, Columbus, Ohio, 43213, United States
Sheila Brooks, Kontakt, [email protected]
Offene Rekrutierung

Pennsylvania

Penn Medicine, Philadelphia, Pennsylvania, 19104, United States
Aktiv, nicht rekrutierend
Allegheny-Singer Research Institute, Pittsburgh, Pennsylvania, 15212, United States
Rachel Reading, Kontakt, [email protected]
Offene Rekrutierung

South Carolina

Medical University of South Carolina, Charleston, South Carolina, 29425, United States
Natalie Koren, Kontakt, [email protected]
Offene Rekrutierung

Texas

UT Southwestern Medical Center, Dallas, Texas, 75390, United States
Aktiv, nicht rekrutierend
UTHealth Houston, Houston, Texas, 77026, United States
Debbie Nguyen, Kontakt, [email protected]
Offene Rekrutierung

Utah

University of Utah Health, Salt Lake City, Utah, 84112, United States
Jordan Esplin, Kontakt, [email protected]
Offene Rekrutierung

Virginia

VCU Medical Center, Richmond, Virginia, 23298, United States
Jinfeng Han, Kontakt, [email protected]
Offene Rekrutierung

Washington

Benaroya Research Institute at Virginia Mason, Seattle, Washington, 98101, United States
Audrey Merz, Kontakt, [email protected]
Offene Rekrutierung
University of Washington, Seattle, Washington, 98105, United States
Mariam Hantouli, MD, Kontakt, 206.543.9662, [email protected]
Kelsey Pullar, MPH, Kontakt, 206.221.8247, [email protected]
Offene Rekrutierung