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Clinical trial

Determination of The 90% Effective Dose of Tegileridine Combined With Propofol for Gastroscopy in Patients of Different Ages: A Biased-Coin Up-and-down Design Study

NCT07678411 is registered in ClinicalTrials.gov with Shiyou Wei as lead sponsor.

NCT NCT07678411
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Registry record

As filed in ClinicalTrials.gov.

Title
Determination of The 90% Effective Dose of Tegileridine Combined With Propofol for Gastroscopy in Patients of Different Ages: A Biased-Coin Up-and-down Design Study
Lead sponsor
Shiyou Wei
Phase
Phase 4
Overall status
Completed
Start date
July 1, 2026
Completion date
July 24, 2026
Enrollment
107 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

painless gastroscopy perioperative sedation, upper gastrointestinal tract lesions