Determinants of Technical Success and Safety in Therapeutic ERCP for Obstructive Jaundice
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: ERCP.
- Who it may be relevant to
- Registry conditions: Obstructive Jaundice, ERCP, Anesthesia Complication, Anesthesia Effectiveness. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Determinants of Technical Success and Safety in Therapeutic ERCP for Obstructive Jaundice: A Prospective Comparative Study.
Overview
compare the impact of type of anesthesia on ERCP including technical success, rate of complications, peri procedural safety, patient and endoscopist satisfaction in adult patients with obstructive jaundice
Interventions
- Procedure ERCP
Effect of anesthesia on Therapeutic ERCP in patients obstructive jaundice
Primary outcome measures
- Impact of type of anesthesia on technical success rate [Time frame: at the time of the procedure]
Secondary outcome measures (1)
- rate of procedure related complications [Time frame: at the time of procedure up to 72 hours post procedure]
Eligibility criteria
Inclusion criteria
- Adult patients above 18 years old.
- Patient with obstructive jaundice as an indication for therapeutic ERCP.
- Provided written informed consent.
Exclusion criteria
- Patients below 18 years old.
- Indications for ERCP other than obstructive jaundice.
- with coagulopathy not corrected prior to procedure.
- severe active cardiopulmonary comorbidities.
- Previous altered upper GIT anatomy (e.g gastric by-pass).
- Pregnancy
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07563569 · Soh-Med-26-4-3MS