Sedation Methods in Percutaneous Transhepatic Biliary Drainage: Procedure Quality and Recovery

Recruiting now · Not applicable

Conditions studied: Fragility, Biliary Obstruction, Cholangitis, Malignancy

In brief

This prospective, randomized, single-center study aims to evaluate and compare two different sedation and analgesia regimens used during percutaneous transhepatic biliary drainage (PTBD) procedures. A total of 96 adult patients undergoing elective PTBD or biliary stenting will be randomized to receive either propofol-remifentanil or propofol-ketamine sedation. The primary outcome is recovery time assessed using the Modified Aldrete Score. Secondary outcomes include procedure quality, pain scores, patient and operator satisfaction, hemodynamic stability, and the incidence of sedation-related adverse events. The study is designed to determine the optimal sedation strategy for PTBD, particularly in fragile and elderly patient populations.

Key facts

Study ID
NCT07640243
Run by
Ankara City Hospital Bilkent
People needed
98
Starts
2026-02-01
Expected to finish
2026-06-10
Last updated by the study team
2026-06-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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