Trials / Unknown
UnknownNCT03942965
Registry Evaluation of a Double Balloon Accessory Device
Multi-center Prospective Registry Study Utilizing a Double Balloon Accessory Device to Facilitate Endoscopic Polypectomy in Large Intestine.
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 165 (actual)
- Sponsor
- Lumendi, LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is collecting standard of care information pertaining to the use of the accessory device and patient outcomes when this double balloon accessory device is used during endoscopic procedures in the colon.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Double balloon accessory device | Double balloon accessory device is used during the endoscopic polypectomy procedure |
Timeline
- Start date
- 2019-01-22
- Primary completion
- 2020-12-31
- Completion
- 2021-03-31
- First posted
- 2019-05-08
- Last updated
- 2020-12-11
Locations
3 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT03942965. Inclusion in this directory is not an endorsement.