Determinants of Technical Success and Safety in Therapeutic ERCP for Obstructive Jaundice
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSohag University
About this trial
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
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients above 18 years old.
Patient with obstructive jaundice as an indication for therapeutic ERCP.
Provided written informed consent.
Disqualifiers
Patients below 18 years old.
Indications for ERCP other than obstructive jaundice.
with coagulopathy not corrected prior to procedure.
severe active cardiopulmonary comorbidities.
Trial design
Design model
Parallel
Treatments tested in this trial
ERCP
Procedure/SurgeryEffect of anesthesia on Therapeutic ERCP in patients obstructive jaundice
Treatment groups
100 Participants
are divided into 2 treatment groupsGroup A: Group AExperimental treatment 1 intervention
Group B: Group BExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Impact of type of anesthesia on technical success rate
Technical success rate defined as successful deep biliary cannulation and completion of the intended therapeutic intervention.
Time frame
at the time of the procedureSecondary outcomes
1
rate of procedure related complications
Procedure related complication exclusively (post ERCP pancreatitis (based on revised Atlanta criteria), bleeding, perforation, cholangitis and aspiration pneumonia)
Time frame
at the time of procedure up to 72 hours post procedureLocations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: