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NCT05172531

Efficacy and Safety Profile of Cisatracurium Besylate for IAH

Status unknown NA Last updated 22 July 2022
What this trial tests

NA trial testing Cisatracurium Besylate in Intra-abdominal Hypertension in 80 participants. Status unknown.

Timeline
29 August 2022
Primary endpoint
30 January 2023
1 April 2023

Quick facts

Lead sponsorTianjin Nankai Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment80
Start date29 August 2022
Primary completion30 January 2023
Estimated completion1 April 2023

Drugs / interventions tested

Conditions studied

Sponsor

Tianjin Nankai Hospital

Who can join

Adults 18 to 90, any sex, with Intra-abdominal Hypertension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a randomized, double-blinded, controlled design. In this study, Cisatracurium Besylate was selected for treatment in Intra-abdominal hypertension or abdominal compartment syndrome,accompanied with evaluating the effects on the duration of organ failure,length of hospital stay and mortality.To clarify the effect of Cisatracurium Besylate on IAH/ACS is of great significance to the clinical applications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Cisatracurium Besylate

Trials testing the same drug.

Other recruiting trials for Intra-abdominal Hypertension

Currently open trials in the same condition.

Other Tianjin Nankai Hospital 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/NCT05172531.

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