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NCT05149430
Quality of Life and Functional Capacity in Post Intensive Care Unit
trial testing Observational Quality of life and functional capacity in Post-intensive Care Syndrome in 101 participants. Completed in 31 March 2020.
30 September 2019
Quick facts
| Lead sponsor | Sanatorio Anchorena San Martin |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 101 |
| Start date | 1 August 2019 |
| Primary completion | 30 September 2019 |
| Estimated completion | 31 March 2020 |
| Sites | 1 location across Argentina |
Drugs / interventions tested
- Observational Quality of life and functional capacity
Conditions studied
- Post-intensive Care Syndrome — all drugs for Post-intensive Care Syndrome →
Sponsor
Sanatorio Anchorena San Martin
Who can join
18 and older, any sex, with Post-intensive Care Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
BACKGROUND. Staying in an intensive care unit can lead to physical and cognitive complications and post-traumatic stress. Currently, the aim is to find out the level of quality of life, functional capacity and cognitive status post intensive care unit. Describe the evolution of the quality of life, functional capacity and cognitive status of a cohort of patients admitted to the ward room after discharge from the intensive care unit, with subsequent follow-up at 3, 6 and 12 months of his discharge. METHODS. Prospective, observational, analytical cohort study. Subjects over 18 years of age with at least 48 hours of confinement in a closed area were included. Demographic variables, quality of life, functional capacity and cognitive status were recorded. A telephone follow-up was carried out three, six and twelve months after institutional discharge. For the evaluation of the primary variables, Euroqol 5d-5L (Eq5d - Eq5d-VAS), Barthel Index and Fototest were used.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT05149430
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Post-intensive Care Syndrome
Currently open trials in the same condition.
- NCT06014931 — Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care · NA · recruiting
Other Sanatorio Anchorena San Martin trials
Trials by the same sponsor.
- NCT07207967 — End-Inspiratory Pause in COPD Patients During Controlled Ventilation · NA · completed
- NCT06195475 — Association Between Tidal Volume and Mortality in Pressure Support in Adults Under Invasive Mechanical Ventilation · completed
- NCT04524091 — Prediction of Inspiratory Effort Response to High PEEP in Patients Recovering From ARDS · recruiting
- NCT04486729 — Respiratory Mechanics and Gas Exchange Characteristics in Patient With SARS-CoV-2 · unknown
- NCT04369105 — Prono Position and Mechanical Power · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05149430 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sanatorio Anchorena San Martin
- Last refreshed: 23 February 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05149430.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing