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Lo studio clinico NCT07358065 per Clinical Application of Dynamic Multimodal Analgesia Regimen After Perianal Abscess Surgery è non ancora in arruolamento. Consulti la vista a schede del Radar degli Studi Clinici e gli strumenti di scoperta IA per tutti i dettagli. Oppure, ponga pure una domanda qui.
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Clinical Application of Dynamic Multimodal Analgesia Regimen After Perianal Abscess Surgery 135 Randomizzato

Non ancora in arruolamento
I dettagli dello studio clinico sono disponibili principalmente in inglese. Tuttavia, Trial Radar IA può essere d'aiuto! Basta cliccare su 'Spiega lo studio' per visualizzare e discutere le informazioni sullo studio nella lingua selezionata.
La sperimentazione clinica NCT07358065 è uno studio interventistico per Clinical Application of Dynamic Multimodal Analgesia Regimen After Perianal Abscess Surgery, attualmente non ancora in arruolamento. L'arruolamento dovrebbe iniziare il 1 gennaio 2026, con l'obiettivo di raggiungere 135 partecipanti. Sotto la guida di The Affiliated Hospital of Putian University, dovrebbe concludersi entro il 31 dicembre 2026. I dati più recenti da ClinicalTrials.gov sono stati aggiornati l'ultima volta il 26 gennaio 2026.
Sommario breve
This study aims to investigate whether the full-course multimodal analgesia regimen based on dynamic assessment (including the integrated traditional Chinese and Western medicine mode) can alleviate postoperative pain, reduce opioid dosage, and decrease the incidence of complications in patients with perianal abscess. It also intends to verify the clinical advantages of the integrated traditional Chinese and Western ...Mostra di più
Titolo ufficiale

Clinical Application of Dynamic Multimodal Analgesia Regimen After Perianal Abscess Surgery

Patologie
Clinical Application of Dynamic Multimodal Analgesia Regimen After Perianal Abscess Surgery
Altri ID dello studio
  • PutianU-014
Numero NCT
NCT07358065
Data di inizio (effettiva)
2026-01-01
Ultimo aggiornamento pubblicato
2026-01-26
Data di completamento (stimata)
2026-12-31
Arruolamento (previsto)
135
Tipo di studio
Interventistico
FASE
N.D.
Stato
Non ancora in arruolamento
Parole chiave
Perianal Abscess
Postoperative Pain
Dynamic Assessment
Multimodal Analgesia
Scopo principale
Altro
Allocazione
Randomizzato
Modello di intervento
In parallelo
Mascheramento
Nessuno (studio in aperto)
Bracci / Interventi
Gruppo/Braccio di partecipantiIntervento/Trattamento
AltroGroup A ：Conventional Analgesia Group
Adopts the traditional analgesic mode.
the traditional analgesic mode
Adopt the traditional analgesic mode: conduct NRS assessment and intervention only when the patient takes the initiative to complain of pain, without fixed assessment time points. Intervene when the pain score is ≥4 points, and no prophylactic medication is administered. Medication use refers to the conventional plan (e.g., flurbiprofen injection, diclofenac sodium capsules, etc.).
AltroGroup B：Western Medicine Multimodal Analgesia Group
Implements a dynamic assessment-based full-course multimodal analgesia strategy.
Western Medicine Multimodal Analgesia
Collect baseline NRS score 24 hours before surgery. After surgery, assess NRS in resting and active states at fixed daily time points (e.g., 08:00, 16:00), and conduct on-demand assessment for breakthrough pain. Reassess during outpatient follow-up at 2 weeks and 1 month after discharge. 1. Stepwise medication intervention: Administer medications in a stepwise manner based on NRS score. For scores ≤3 points, priorit...Mostra di più
AltroGroup C：Integrated Traditional Chinese and Western Medicine Multimodal Analgesia Group
Integrates characteristic traditional Chinese medicine nursing interventions on the basis of western medicine multimodal analgesia.
Integrated Traditional Chinese and Western Medicine Multimodal Analgesia
On the basis of western medicine multimodal analgesia, integrate characteristic traditional Chinese medicine nursing interventions, such as auricular point pressing, wrist-ankle acupuncture, traditional Chinese medicine sitz bath, etc.
Esito primario
Misure di esitoDescrizione della misuraArco temporale
Postoperative pain score
Postoperative pain score (NRS，Numeric Rating Scale): Record pain scores at rest and during activity on postoperative days 1, 2, 3, 4, 5, as well as at 2 weeks and 1 month after discharge, serving as the core assessment of the analgesic effect of the regimen.NRS，0 points indicate no pain, while 10 points represent the most severe pain.
From enrollment to 1 month after discharge
Esito secondario
Misure di esitoDescrizione della misuraArco temporale
Secondary Efficacy Indicators
Total postoperative analgesic consumption: Convert all analgesics to morphine equivalent dose (MEDD) for intergroup comparison to evaluate the opioid-sparing effect of the regimen.
From enrollment to 1 month after discharge
Assistente alla partecipazione
Criteri di eleggibilità

Età idonea
Adulto, Adulto anziano
Età minima
18 Years
Sessi idonei
Tutti
  • Diagnosed with primary perianal abscess by clinical examinations (digital rectal examination, ultrasound, or MRI) and undergoing incision and drainage or radical surgical treatment;
  • Abscess diameter ≥ 2 cm or accompanied by obvious abscess cavity formation;
  • Patients are willing and able to participate in the pain management plan, understand the importance of pain management, and actively cooperate;
  • No severe coagulation disorders.

  • Complicated with specific infectious diseases such as Crohn's disease or tuberculosis;
  • Unclear source of postoperative pain (i.e., the patient's pain is uncertain or unrelated to the surgery);
  • Having definite contraindications, including drug allergies or inability to accept certain pain management methods adopted in the study;
  • Pregnant or lactating women;
  • Patients unable to cooperate with the study, such as those with cognitive impairment, history of mental illness, or communication difficulties;
  • Patients with long-term use of analgesic drugs and developed drug tolerance;
  • Complicated with uncontrolled cardiovascular and cerebrovascular diseases (NYHA cardiac function Class Ⅲ-Ⅳ), liver or kidney insufficiency (Child-Pugh Class C or eGFR < 30 ml/min/1.73m²), etc.;
  • Abscess secondary to rectal tumors, trauma, or iatrogenic injury;
  • Postoperative occurrence of severe complications (e.g., massive hemorrhage, sepsis) or combined infection in other parts;
  • Patients receiving only non-surgical treatments such as simple puncture and aspiration of pus.
The Affiliated Hospital of Putian University logoThe Affiliated Hospital of Putian University
Parte responsabile dello studio
Hong Wu, Investigatore principale, Supervisory assistant of Scientific Research Department, The Affiliated Hospital of Putian University
Contatti principali dello studio
Contatto: Yanbing Ye, +8613959528973, [email protected]
1 Centri dello studio in 1 paesi

Fujian

Affiliated Hospital of Putian University, Putian, Fujian, China