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NCT03208023: RESIPI

RESIPI for Reducing Perioperative Major Adverse Cardiac Events

Terminated NA Last updated 17 November 2022
What this trial tests

NA trial testing RESIPI Management Strategy in Inotropy in 155 participants. Terminated before completion.

Timeline
9 October 2017
Primary endpoint
1 November 2018
3 December 2018

Quick facts

Lead sponsorVanderbilt University Medical Center
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment155
Start date9 October 2017
Primary completion1 November 2018
Estimated completion3 December 2018
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Vanderbilt University Medical Center

Who can join

18 and older, any sex, with Inotropy or Fluid Management. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to evaluate the effect of a novel hemodynamic management and monitoring strategy for reducing cardiac bio marker elevations and major adverse cardiac events.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Vanderbilt University Medical Center 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/NCT03208023.

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