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RecruitingNCT07490132Updated Mar 24, 2026

Endoscopic Retrograde Cholangiopancreatography

An observational study in Gastro-Intestinal Disorder, sponsored by Methodist Health System. Recruiting at 1 site in United States. Open to participants aged 15 Years and older. Per ClinicalTrials.gov, last updated 2026-03-24.

Sponsored by Methodist Health System · Observational

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Study type
Observational
Model
Case-only
Time perspective
Other
Enrollment
100
Ages
15 Years and older
Sex
All
01

Study summary

The risk of post-endoscopic retrograde cholangiopancreatography(ERCP) pancreatitis(PEP) is influenced by patient and procedure-related factors. Strategies to decrease PEP(Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis) are of great importance.

Read the detailed description

The primary objective of this study is to provide a mechanism to store the following information about patients undergoing ERCPs at Methodist Dallas Medical Center. This registry will be permissive of quality improvement and research studies.

02

Conditions studied

  • Gastro-Intestinal Disorder
03

In context

Digestive System Diseases

406 studies on the registry are indexed under Digestive System Diseases; 79 are open to participants now.

This study's planned enrollment of 100 is below the median of 400 across 105 observational studies indexed under Digestive System Diseases.

Browse Digestive System Diseases studies →

Lead sponsor

Methodist Health System is the lead sponsor of 170 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients who underwent ERCP and in MDI(Methodist Digestive Institute) registry.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Patients >15 years Included in MDI's Registry Underwent ERCP between January 1, 2000 through December 31, 2025

Exclusion criteria

Exclusion Criteria:

Patients \<15 years Patients in which cannulation was via a surgical anastomosis Patients in which cannulation was not attempted due to gastric outlet obstruction, the main papilla not found, or the minor papilla was not found will be excluded.

05

Study design

Observational model
Case-only
Time perspective
Other
Enrollment
100 participants (estimated)
Target follow-up
25 Years
Patient registry
Yes

Groups and cohorts

  • Underwent ERCP

    Underwent ERCP between January 1, 2000 through December 31, 2025

    Other: Patients undergoing ERCPs at Methodist Dallas Medical Center

Interventions

  • OtherPatients undergoing ERCPs at Methodist Dallas Medical Center

    The registry will include all patients who meet registry inclusion. Enrollment will terminate once 25 years of data are captured: January 1, 2000 through December 31, 2025.

06

What researchers measure

Primary outcomes

  1. Underwent ERCP

    Patients undergoing ERCPs at Methodist Dallas Medical Center.

    Time frame: 25 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — The investigator will make all possible efforts to ensure compliance with all policies regarding sharing of Protected Health Information or research information. Only de-identified Protected Health Information will be shared in relevant research mediums.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Feb 2026; primary completion for Feb 2027, 12 months later.

Of 45 non-industry observational studies under Digestive System Diseases, half reached primary completion within 46 months of starting (the median), counting those still running; a quarter within 18 and three quarters within 114. This study's planned 12 months is below that.

Counting every sponsor, half of 56 studies reached it within 43 months; a quarter within 18 and three quarters within 102.

Digestive System Diseases covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 18, 2026
First posted
Mar 24, 2026
StartEst.
Feb 2026
Primary completionEst.
Feb 2027
CompletionEst.
Feb 2028
Last update
Mar 24, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 24, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07490132
Responsible party
Sponsor
First posted
Mar 24, 2026
Start date
Feb 2026 (estimated)
Primary completion
Feb 2027 (estimated)
Completion
Feb 2028 (estimated)
Last update
Mar 24, 2026

Study contacts

Crystee Cooper, DHEd
Contact
ClinicalResearch@mhd.com
214-947-1280
Kavya Mankulangara
Contact
ClinicalResearch@mhd.com
214-947-4604
Prashant Kedia, MD
principal investigator · Methodist Health System

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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