RECRUITING

Prospective Evaluation of the Efficacy and Safety of Endoscopic Tissue Apposition

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study is a prospective registry of patients undergoing endoscopic suturing and/or clip placement at our institution to assess the efficacy and safety of endoscopic tissue apposition. 1.1 Hypothesis: Endoscopic tissue apposition is efficacious and safe in the practice of gastrointestinal endoscopy. 1.2 Aims: To prospectively evaluate the efficacy and safety of Endoscopic Tissue Apposition in the practice of gastrointestinal endoscopy.

Official Title

Prospective Evaluation of the Efficacy and Safety of Endoscopic Tissue Apposition

Quick Facts

Study Start:2016-12-12
Study Completion:2026-12-16
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03626194

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients\>18 years of age undergoing endoscopy for any of the following indications:
  2. * Closure of perforations
  3. * Closure of full thickness defects created during endoscopic full thickness resection
  4. * Closure of defects after endoscopic submucosal dissection and endoscopic mucosal resection
  5. * Closure of mucosotomy after Peroral Endoscopic Myotomy (POEM)
  6. * Stent fixation
  7. * Closure of fistulas
  8. * Natural Orifice Transluminal Endoscopic Surgery defect closures
  9. * Post-bariatric surgery gastrojejunal anastomosis and gastric pouch revision (transoral outlet repair)
  10. * Primary endoscopic sleeve gastroplasty
  1. * Patients unable or unwilling to provide consent
  2. * Pregnant patients
  3. * Coagulation disorders (INR \>1.8, platelet \<50,000)
  4. * GI Bleeding
  5. * Hemodynamic instability
  6. * Enrollment in another device or drug study that may confound the results

Contacts and Locations

Study Contact

Abigail Lowe
CONTACT
303-724-6070
ABIGAIL.LOWE@UCDENVER.EDU

Study Locations (Sites)

University of Colorado Hospital
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2016-12-12
Study Completion Date2026-12-16

Study Record Updates

Study Start Date2016-12-12
Study Completion Date2026-12-16

Terms related to this study

Additional Relevant MeSH Terms

  • Endoscopic Tissue Apposition
  • Endoscopic Suturing
  • Endoscopic Clipping
  • Bariatric Endoscopy
  • Transoral Outlet Reduction
  • Endoscopic Sleeve Gastroplasty