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NCT03196479

Comparison Between Efficacy of Ketamine and Propofol Mixture With 1:6 Ratio and 1:4 Ratio for Endoscopic Retrograde Procedure Sedation

Completed NA Last updated 6 September 2017
What this trial tests

NA trial testing ketamine and propofol mixture with 1:6 ratio in Adult Patients Undergoing ERCP in 58 participants. Completed in 31 August 2017.

Timeline
1 March 2017
Primary endpoint
30 June 2017
31 August 2017

Quick facts

Lead sponsorIndonesia University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment58
Start date1 March 2017
Primary completion30 June 2017
Estimated completion31 August 2017
Sites1 location across Indonesia

Drugs / interventions tested

Conditions studied

Sponsor

Indonesia University

Who can join

Adults 18 to 65, any sex, with Adult Patients Undergoing ERCP. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aimed to compare the efficacy of ketamine and propofol mixture with 1:6 ratio and 1:4 ratio for endoscopic retrograde procedure

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Indonesia University trials

Trials by the same sponsor.

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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/NCT03196479.

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