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Post-ERCP Cholecystectomy. How ERCP and ERCP-related Variables Effect the Outcomes?

NCT06388525 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 426

Last updated 2024-04-29

No results posted yet for this study

Summary

In this retrospective study, we aimed to detect of effects of ERCP on outcomes of Laparoscopic Cholecystectomy. Patients underwent elective cholecystectomy surgery with a diagnosis of symptomatic cholelithiasis were identified and divided into two main groups regarding to have a ERCP procedure prior to surgery or not. To eliminate possible differences in baseline characteristics, patients in ERCP and non-ERCP groups were propensity score-matched 1:1 using nearest-neighbor matching without replacement based on age, sex and ASA score. Following propensity score matching (PSM), the ERCP and non-ERCP groups were first compared to detect effects of the ERCP procedure itself. After comparison of two main groups, subgroup analyzes performed for the ERCP group to detect effect of ERCP-related variables (indication for ERCP procedure, time between last ERCP procedure and surgery, number of preoperative ERCPs, stone extractions, and biliary stent use)

Conditions

  • Endoscopic Retrograde Cholangiopancreatography
  • ERCP-Laparoscopic Cholecystectomy Interval
  • Number of Preoperative ERCPs
  • Stone Extraction Status in ERCP Procedures
  • Biliary Stents
  • Mechanical Lithotripsy

Interventions

PROCEDURE

Endoscopic Retrograde Cholangiopancreatography

Sponsors & Collaborators

  • Kanuni Sultan Suleyman Training and Research Hospital

    lead OTHER

Principal Investigators

  • Yasir Musa Kesgin · Istanbul Kanuni Sultan Suleyman Training and Research Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2020-01-01
Completion
2020-01-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06388525 on ClinicalTrials.gov