Sedation Methods in Percutaneous Transhepatic Biliary Drainage: Procedure Quality and Recovery
Recruiting
N/A
Interventional Study
Fragility
Biliary Obstruction
Cholangitis
Malignancy
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 98 (estimated)
- Sponsor
- Ankara City Hospital Bilkent · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Scheduled for elective percutaneous transhepatic biliary drainage (PTBD) and/or biliary stenting
* ASA physical status II-IV
* Fasting time of at least 6 hours prior to the procedure
* Ability to provide written informed consent
Exclusion Criteria:
* Inability to provide inf…
Contacts
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