Registry for patients undergoing percutaneous cholangiopancreatoscopy
The Percutaneous Cholangiopancreatoscopy Registry
This study is collecting information from patients who have had a procedure called percutaneous cholangiopancreatoscopy to see how well it works and what outcomes people experience.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 540 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Johns Hopkins University Academic / other |
| Locations | 1 site (Baltimore, Maryland) |
| Trial ID | NCT05210322 on ClinicalTrials.gov |
What this trial studies
The Percutaneous Cholangiopancreatoscopy (PCPS) registry is an observational registry that collects data from patients undergoing the percutaneous cholangiopancreatoscopy procedure across multiple sites in the United States. It includes both retrospective data collection from past patients and prospective enrollment of new patients over a three-year period. The goal is to gather comprehensive clinical and procedural information to better understand the outcomes and effectiveness of this procedure.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are undergoing clinically indicated percutaneous cholangiopancreatoscopy procedures.
Not a fit: Patients who are pregnant or under 18 years of age will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance the understanding of percutaneous cholangiopancreatoscopy outcomes, leading to improved patient care and treatment strategies.
How similar studies have performed: While this registry approach is observational, similar studies have successfully gathered data to improve clinical practices in other medical fields.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Male or female adults * 18 years of age and older * Patients undergoing clinically indicated percutaneous cholangiopancreatoscopy procedure at the Johns Hopkins Hospital or one of the registry sites. * Willing and able to understand and sign a written informed consent document for the prospective component of the study. Exclusion Criteria: * Pregnant women * Children (\< 18 years of age)
Where this trial is running
Baltimore, Maryland
- Johns Hopkins Hospital — Baltimore, Maryland, United States (Recruiting)
Study contacts
- Principal investigator: Harjit Singh, MD — Johns Hopkins University
- Study coordinator: Harjit Singh, MD
- Email: hsingh@jhmi.edu
- Phone: 4432872915
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.