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L'essai clinique NCT06751888 (CO2-nOH) pour Hypotension orthostatique neurogène est pas encore en recrutement. Consultez la vue en carte du Radar des Essais Cliniques et les outils de découverte par IA pour tous les détails, ou posez vos questions ici.
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Controlled CO2 Inhalation in NOH (CO2-nOH)

Pas encore en recrutement
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L'étude clinique NCT06751888 (CO2-nOH) est un essai interventionnel pour Hypotension orthostatique neurogène. Son statut actuel est : pas encore en recrutement. Le recrutement est prévu pour commencer le 1 mai 2025, avec un objectif de 28 participants. Dirigé par l'Université de Calgary, l'essai devrait être terminé d'ici le 31 décembre 2028. Les données du site ClinicalTrials.gov ont été mises à jour pour la dernière fois le 30 décembre 2024.
Résumé succinct
This study focuses on neurogenic orthostatic hypotension (nOH), which is a disorder characterized by an abnormal drop in blood pressure (BP) within 3-minutes of standing. Patients with nOH experience debilitating symptoms including light-headedness, falls, and fainting. Patients often struggle with day-to-day tasks that require standing, with a reduced quality-of-life. Current therapies for nOH have limited effectiveness and unwanted side effects. Our lab has found that raising blood CO2 levels (hypercapnia) in the lab increases BP when standing in patients with nOH. We now aim to test the CarboHaler, an exogenous controlled CO2 delivery device, in this study to see if increasing CO2 levels through controlled CO2 inhalation can improve BP and reduce symptoms in patients with nOH when standing up. On the study day, participants will undergo two Head-up Tilt (HUT; upright) tests with different breathing protocols: one with and one without exogenous CO2 delivery provided by a CO2 inhalational device. We will record heart rate, blood pressure, and breathing parameters. We will also assess upright symptoms using the Vanderbilt Orthostatic Symptoms Score. Our primary outcome is the magnitude of the change in systolic BP from lying down to standing, which will be compared with and without exogenous CO2 delivery. We hypothesize that exogenous CO2 delivery provided by a CO2 inhalational device will raise CO2 enough to increase standing BP, which could reduce the debilitating symptoms experienced by patients with nOH. We hope that these data will support future clinical trials, with the long-term goal of creating a simple, low-cost treatment for increasing quality-of-life for patients with nOH.
Titre officiel

Controlled CO2 Inhalation to Increase Blood Pressure in Neurogenic Orthostatic Hypotension: a Proof-of-Concept Novel Therapy Study

Conditions
Hypotension orthostatique neurogène
Autres identifiants de l'essai
  • CO2-nOH
  • REB24-1780
Numéro NCT
Date de début (réel)
2025-05-01
Dernière mise à jour publiée
2024-12-30
Date de fin (estimée)
2028-12-31
Inscription (estimée)
28
Type d'essai
Interventionnel
PHASE
N/A
Statut
Pas encore en recrutement
Mots clés
Neurogenic Orthostatic Hypotension
Autonomic
Cardiovascular
Therapies
Quality-of-life
Symptom-management
Novel
Objectif principal
Traitement
Plan d'attribution
Randomisé
Modèle d'intervention
Croisé
Masquage
Simple aveugle
Bras / Interventions
Groupe de participants/BrasIntervention/Traitement
Comparateur factice0% CO2 Arm
In this arm, participants will breathe with the CO2 delivery device providing no exogenous CO2 while supine and during a 10-min HUT test.
Controlled CO2 Delivery (Sham)
For this intervention, we will be using this device set at 0% CO2 for our sham comparison.
ExpérimentalControlled CO2 Inhalation Arm
In this arm, participants will breathe with the CO2 delivery device in the supine position until BP levels increase. Once a BP increase is observed, participants will be tilted upright and will continue to breathe with the inhalation device during a 10-min HUT test.
Controlled CO2 Delivery
The use of a controlled CO2 delivery offers a straightforward way to increase arterial CO2. Controlled CO2 inhalation may offer a novel hemodynamic therapy for patients with Neurogenic Orthostatic Hypotension
Critère principal d'évaluation
Critères d'évaluationDescription de critèresPériode
Magnitude of the systolic blood pressure (SBP) response
The primary outcome measures will be the magnitude of the systolic blood pressure (SBP) response (ΔSBP = Head Up Tilt - Supine) during 0% CO2 vs. Controlled CO2 inhalation.
Start of in-lab study day to the end of the in-lab study day
Critère secondaire d'évaluation
Critères d'évaluationDescription de critèresPériode
Change in Cerebral Blood Flow (ΔCBFv)
Secondary outcome measures will be the change in Cerebral Blood Flow (ΔCBFv) for each arm of the study.
Start of in-lab study day to the end of the in-lab study day
Change in Vanderbilt Orthostatic Symptom Scores (ΔVOSS)
Secondary outcome measures will be the change in Vanderbilt Orthostatic Symptom Scores (ΔVOSS) for each arm of the study.
Start of in-lab study day to the end of the in-lab study day
Critères d'éligibilité

Âges éligibles
Adulte, Adulte âgé
Âge minimum
18 Years
Sexes éligibles
Tous
  • Age ≥18 years
  • Male and Female
  • Physician diagnosis of Neurogenic Orthostatic Hypotension
  • Non-smokers.
  • Able and willing to provide informed consent.
  • Ability to travel to Libin Cardiovascular Institute Autonomic Testing Lab at the University of Calgary, Calgary, AB.

  • Pregnant or breast-feeding females
  • Subjects with chronic heart failure or severe pulmonary disease who are unable to climb one flight of stairs due to shortness of breath.
  • Presence of failure of other organ systems or systemic illness that can affect autonomic function or the participant's ability to cooperate. These include dementia, alcohol and/or drug abuse.
  • Other factors which in the investigator's opinion would prevent the participant from completing the protocol, including poor compliance during previous studies.
Aucune donnée de contact disponible
1 Centres de l'essai dans 1 pays

Alberta

University of Calgary, Calgary, Alberta, T2N 4Z6, Canada
Satish Raj, MD MSCI, Contact, 4032106152, [email protected]
Rasha Hamzeh, RN, Contact, 4032208897, [email protected]