Registry for advanced endoscopic procedures in gastrointestinal conditions
Research Registry for Endoscopic Treatment and Diagnostics
This study is collecting information from patients who are getting special endoscopic procedures for serious gastrointestinal conditions to see how well these treatments work.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Region Stockholm Government |
| Locations | 1 site (Stockholm) |
| Trial ID | NCT05187312 on ClinicalTrials.gov |
What this trial studies
This observational registry collects data on patients undergoing endoscopic diagnostic and therapeutic interventions for conditions such as cholangiocarcinoma, pancreatic cancer, and sclerosing cholangitis. The study aims to document the outcomes and effectiveness of procedures like endoscopic retrograde cholangiopancreatography and endoscopic ultrasound. By gathering comprehensive data, the registry seeks to enhance understanding and improve future treatment strategies for these serious gastrointestinal diseases.
Who should consider this trial
Good fit: Ideal candidates for this registry are patients with a clinical indication for endoscopic intervention who are able to provide informed consent.
Not a fit: Patients under 18 years of age or those unable to provide informed consent will not benefit from this registry.
Why it matters
Potential benefit: If successful, this registry could lead to improved treatment protocols and outcomes for patients with advanced gastrointestinal conditions.
How similar studies have performed: Other observational registries in similar gastrointestinal conditions have shown success in improving patient outcomes and treatment approaches.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Clinical indication for endoscopic intervention/procedure Exclusion Criteria: * No informed consent * Age \<18 years
Where this trial is running
Stockholm
- Karolinska University Hospital — Stockholm, Sweden (Recruiting)
Study contacts
- Principal investigator: Erik von Seth, MD, PhD — Region Stockholm
- Study coordinator: Erik von Seth, MD, PhD
- Email: erik.von.seth@ki.se
- Phone: +46812380000
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.