Small Bowel Diseases Clinical Trial
Official title:
A Double Blind, Placebo Controlled, Randomized Cross Over Study of an Enteroscope Stiffening Device to Increase Terminal Ileum Intubation Rate During Retrograde Balloon Assisted Enteroscopy
Balloon assisted enteroscopy has revolutionized the management of small bowel diseases by enabling endoscopic access deep into the small bowel. Using a combination of antegrade (through the mouth) and retrograde (through the anus) approaches, a large portion of the small bowel can be examined. Access to the proximal small bowel through the pylorus using the antegrade approach is straightforward but intubating the distal small bowel through the ileocecal valve is challenging due to the flexibility of the enteroscope. Recently, an enteroscopy stiffening wire has been developed. The purpose of our double blind placebo controlled randomized cross over study is to evaluate the performance of the enteroscopy stiffening wire in achieving terminal ileum intubation (TI) during retrograde balloon assisted enteroscopy.
| Status | Suspended |
| Enrollment | 46 |
| Est. completion date | December 2019 |
| Est. primary completion date | December 2019 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 14 Years and older |
| Eligibility |
Inclusion Criteria: 1. Patients undergoing retrograde balloon assisted enteroscopy (either SBE or DBE) for management of small bowel diseases. Exclusion Criteria: 1. Age < 14 2. Prior ileocecal surgery, resection, or anastomosis 3. Inability to reach the cecum during retrograde balloon assisted enteroscopy 4. Hemodynamic instability 5. Inpatient procedure |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Diagnostic
| Country | Name | City | State |
|---|---|---|---|
| Canada | London Health Sciences Center-Victoria Campus | London | Ontario |
| Lead Sponsor | Collaborator |
|---|---|
| Lawson Health Research Institute |
Canada,
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Peri-procedural adverse events | Within the first 24 hours of the procedure | Yes | |
| Other | Adverse events within the first 7 days | Between 1-7 days of the procedure | Yes | |
| Primary | Terminal ileum intubation rate | Intraoperative | No | |
| Secondary | Terminal ileum intubation time for successful intubations | Intraoperative | No | |
| Secondary | Small bowel diagnostic rate | Intraoperative | No | |
| Secondary | Small bowel intervention rate | Intraoperative | No |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT02334631 -
High Volume Simethicone VCE Clinical Trial
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Phase 4 |