Actively Recruiting

Age: 15Years +
All Genders
ID07490132

Endoscopic Retrograde Cholangiopancreatography Patient Registry Observational Study at Methodist Dallas Medical Center

Led by Methodist Health System · Updated on 2026-03-24

100

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect and store detailed information about patients who undergo Endoscopic Retrograde Cholangiopancreatography (ERCP) procedures at Methodist Dallas Medical Center. The study focuses on factors influencing the risk of pancreatitis following ERCP, a serious complication, and supports quality improvement and research efforts related to gastro-intestinal disorders. Patients included in this registry are those who had ERCP performed at the center between January 1, 2000, and December 31, 2025. The study gathers data permissively for up to 25 years to monitor patient outcomes and procedural details. No specific treatments or interventions are assigned; instead, data from past and future ERCP cases are collected for observational purposes. Participants' information, including procedural records and outcomes, will be stored and analyzed to understand risks and improve care. The primary measure is the inclusion of patients who underwent ERCP over the 25-year period. The study does not involve additional interventions or treatment changes and will continue data collection until the end date in February 2028.

CONDITIONS

Brief Title

Endoscopic Retrograde Cholangiopancreatography

Who Can Participate

Age: 15Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 15 years or older
  • Underwent Endoscopic Retrograde Cholangiopancreatography (ERCP) between January 1, 2000 and December 31, 2025
  • Included in Methodist Dallas Medical Center's registry
Not Eligible

You will not qualify if you...

  • Patients younger than 15 years
  • Cannulation performed via a surgical anastomosis
  • Cannulation not attempted due to gastric outlet obstruction
  • Main papilla not found during procedure
  • Minor papilla not found during procedure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to 25 years

Participants undergo Endoscopic Retrograde Cholangiopancreatography (ERCP) procedures as part of routine clinical care.

Visits occur as participants undergo ERCP procedures between January 1, 2000 and December 31, 2025

Long-term Monitoring

Duration - Up to 25 years

Participants who undergo routine care are observed through data collection in the registry over time.

Trial Site Locations

Total: 1 location

1

Methodist Dallas Medical Center- Clinical Research Institute

Dallas, Texas, United States, 75203

Actively Recruiting

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Research Team

C

Crystee Cooper, DHEd

K

Kavya Mankulangara

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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