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NCT04489589: LIBERATE
Midodrine for the Early Liberation of Vasopressor Support in the ICU
Phase 4 trial testing Midodrine in Critical Illness in 20 participants. Completed in 30 October 2022.
31 July 2022
Quick facts
| Lead sponsor | University of Alberta |
|---|---|
| Phase | Phase 4 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | treatment |
| Enrollment | 20 |
| Start date | 22 March 2021 |
| Primary completion | 31 July 2022 |
| Estimated completion | 30 October 2022 |
| Sites | 1 location across Canada |
Drugs / interventions tested
- Midodrine — full drug profile →
- Placebo
Conditions studied
- Critical Illness — all drugs for Critical Illness →
- Shock — all drugs for Shock →
Sponsor
University of Alberta
Who can join
18 and older, any sex, with Critical Illness or Shock. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Vasopressors are medications that are given intravenously to increase the blood pressure of patients with illnesses that cause dangerous blood pressure drops. When a doctor prescribes a vasopressor, they ask that the dose be adjusted to achieve a specific blood pressure. This kind of medical support with intravenous (IV) vasopressors are usual treatments in intensive care unit (ICU) settings. Oral vasopressors, such as midodrine, have been historically used to maintain blood pressure in non-critically ill patients. In this study, the investigators will be using midodrine to reduce the need for IV vasopressors as blood pressure improves during the stay in the ICU The LIBERATE pilot study will evaluate the role of midodrine for patients with low blood pressure in the ICU. The investigators are planning on enrolling up to 20 study participants to evaluate this question in the General Systems ICU at the University of Alberta Hospital.
Publications & conference data
3 peer-reviewed publications reference this trial (live from Europe PMC):
-
Impact of Adjuvant Use of Midodrine to Intravenous Vasopressors: A Systematic Review and Meta-Analysis.
Al-Abdouh A, Haddadin S, Matta A, Jabri A, et al · · 2021 · cited 9× · PMID 34055408 · DOI 10.1155/2021/5588483 -
LIBERATE: a study protocol for midodrine for the early liberation from vasopressor support in the intensive care unit (LIBERATE): protocol for a randomized controlled trial.
Opgenorth D, Baig N, Fiest K, Karvellas C, et al · · 2022 · cited 4× · PMID 35246227 · DOI 10.1186/s13063-022-06115-0 -
Midodrine for the early liberation from vasopressor support in the ICU (LIBERATE): a feasibility study.
Kilcommons SJ, Hammal F, Opgenorth DL, Fiest KM, et al · · 2024 · cited 1× · PMID 39633467 · DOI 10.1186/s40814-024-01577-2
Verify or expand the search:
- PubMed search for NCT04489589
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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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 NCT04489589 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Alberta
- Last refreshed: 6 October 2023
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/NCT04489589.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing