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NCT02990546

Midodrine in the Recovery Phase of Septic Shock

Withdrawn Phase 3 Last updated 11 January 2024
What this trial tests

Phase 3 trial testing midodrine in Septic Shock. Withdrawn.

Timeline
1 March 2017
Primary endpoint
2 May 2018
2 May 2018

Quick facts

Lead sponsorUniversity of Virginia
PhasePhase 3
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Start date1 March 2017
Primary completion2 May 2018
Estimated completion2 May 2018
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Virginia

Who can join

18 and older, any sex, with Septic Shock. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of this study is to investigate the role of oral midodrine in the recovery of septic shock. The investigators hypothesize that the oral drug can reduce central line days and ICU length of stay.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of midodrine

Trials testing the same drug.

Other recruiting trials for Septic Shock

Currently open trials in the same condition.

Other University of Virginia trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT02990546.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing