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NCT05517408

Dose Exploration of Ciprofol for Sedation in Gastrointestinal Endoscopic Diagnosis and Treatment of Obese Patients.

Status unknown NA Last updated 16 August 2023
What this trial tests

NA trial testing ciprofol in Gastric Cancer in 30 participants. Status unknown.

Timeline
19 September 2022
Primary endpoint
3 November 2022
13 August 2023

Quick facts

Lead sponsorRenJi Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment30
Start date19 September 2022
Primary completion3 November 2022
Estimated completion13 August 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

RenJi Hospital

Who can join

Adults 18 to 60, any sex, with Gastric Cancer or Gastric Ulcer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Ciprofol is a new anesthetic, which combines with γ- Aminobutyric acid-a (GABAA) receptor. Ciprofol has shown equivalent anesthetic efficacy of propofol at 1/4 to 1/5 of the dosage. Ciprofol has the pharmacodynamic characteristics of rapid onset, stable and rapid recovery. Phase III clinical results showed that the incidence of injection pain and respiratory and circulatory depression of ciprofol was lower than that of propofol. Therefore, ciprofol has a good application prospect in sedation for gastrointestinal endoscopy, especially for obese patients. In the current study, we would explore the proper dose of Ciprofol in sedated gastrointestinal endoscopy in obese patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of ciprofol

Trials testing the same drug.

Other recruiting trials for Gastric Cancer

Currently open trials in the same condition.

Other RenJi 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/NCT05517408.

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