Comparison Between Pre and Intraoperative ERCP in Treatment of Common Bile Duct Stones

NCT ID: NCT01046552

Last Updated: 2010-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

210 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-06-30

Study Completion Date

2009-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

ERCP plays an important role in management of common bile duct stones. Herein the investigators compare preoperative against intraoperative ERCP.

210 were included but only 198 patients were randomly divided into two groups; PES/LC (100 patients) and LC/IOES (98 patients).

The total hospital stay were significantly shorter in the group of LC/IOES

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Common Bile Duct Stones.

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

PES/LC

preoperative ES followed by LC within the same hospital admission

Group Type ACTIVE_COMPARATOR

preoperative ERCP and LC

Intervention Type PROCEDURE

preoperative ERCP followed by LC

LC/IOES

laparoscopic cholecystectomy with intraoperative ercp under the same anesthesia

Group Type ACTIVE_COMPARATOR

Intraoperative ERCP and LC

Intervention Type PROCEDURE

LC and intraoperative ERCP

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

preoperative ERCP and LC

preoperative ERCP followed by LC

Intervention Type PROCEDURE

Intraoperative ERCP and LC

LC and intraoperative ERCP

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* patients with gallstones and common bile duct stones

Exclusion Criteria

* contraindications to ercp

contraindication to laparoscopy

biliary pancreatitis

refusal to participate
Minimum Eligible Age

12 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Mansoura University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

gastroenterology surgical center

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ahmed Abdel-Raouf El-Geidie

Al Mansurah, Dakahlia Governorate, Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Related Links

Access external resources that provide additional context or updates about the study.

http://www.mans.edu.eg

mansoura university

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ERCP123

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.