CTRI/2020/09/027589
Not Yet Recruiting
N/A
Artificial Breathing Capability Device (ABCD): Design, Development, Testing and Clinical Validation - ABCD Trial
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Health Condition 1: J22- Unspecified acute lower respiratory infection
- Sponsor
- Department of Science and Technology
- Status
- Not Yet Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Any patient admitted with respiratory failure deemed by the treating team to require manual ventilation with Ambu bag (because of non\-availability of a ventilator), for any clinical condition including respiratory failure due to respiratory diseases, neurologic diseases, intoxication or poisoning.
Exclusion Criteria
- •Patients on a mechanical ventilator.
- •patient undergoing procedures such as resuscitation attempts, surgery, or other life\-saving procedures.
- •Patients deemed to be unsuitable for manual ventilation (for any reason) by the treating team.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not Yet Recruiting
N/A
Clinical trial to study the convenience and usability of newly proposed adaptive positive airway pressure mask for obstructive sleep apneaCTRI/2024/04/066167Department of Science and Technology
Recruiting
N/A
Respiratory Support System Triggered by Bio-impedance and Myography for Preterms and NeonatesP28.4Other apnoea of newbornDRKS00016470niversitätsklinikum Leipzig40
Completed
N/A
How device assisted regulation of normal breath changes the autonomic functions in patients with non-communicable lifestyle conditionsHealth Condition 1: I10- Essential (primary) hypertensionHealth Condition 2: E663- OverweightHealth Condition 3: E119- Type 2 diabetes mellitus without complicationsCTRI/2021/11/038289Patanjali Research Foundation Trust300
Completed
N/A
Bronchodilator response in COPD: absent or wrong method of measurement?Chronic obstructive pulmonary diseaseRespiratory - Chronic obstructive pulmonary diseaseACTRN12605000304639Woolcock Institute of Medical Research30
Active, Not Recruiting
N/A
avage Bronchiolo-Alvéolaire sous ventilation non Invasive et sédation intra veineuse en objectif de concentration au Propofol chez le malade en insuffisance Respiratoire Aiguë.Etude Randomisée Contrôlée - SEDA-FIBROPatient présentant une Insuffisance Respiratoire Aigüe avec nécessité d'une fibroscopie bronchique avec Lavage Bronchiolo-Alvéolaire.MedDRA version: 9.1Level: LLTClassification code 10001053Term: Acute respiratory failureEUCTR2008-000757-35-FRCHU de Bordeaux