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NCT03939819 · ClinicalTrials.gov registry record · NA
Endoscopic vs. Suction Device Calibration in Sleeve Gastrectomy
A NA study, sponsored by Emory University.
- Completed
- Registry status
- NA
- Development phase
- 106
- Enrollment target
NCT03939819: Completed NA study, sponsored by Emory University.
NCT03939819 is a NA study that has completed, run by Emory University. The registered enrollment target is 106 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03939819, a NA study, has completed, sponsored by Emory University.
- COMPLETED
- Registry status
- NA
- Development phase
- 106 participants
- Enrollment target
Study Summary
This study aims to compare the difference in staple usage and post-operative GERD (heartburn) between patients that had an endoscope used versus patients that had a suction calibration system used on them during "laparoscopic sleeve gastrectomy" (LSG).
Primary Outcome
Staple usage will be recorded during the weight loss surgery procedure.
Interventions
- DEVICE ViSiGi® 3D suction calibration device
- DEVICE Esophagogastroduodenoscopy (EGD) calibration
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2019-07-30 |
| Est. Completion | 2022-02-02 |
| Phase | NA |
What the finished NCT03939819 record still lists
NCT03939819 is an interventional study that assigns participants to a tested intervention. The registered 106 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 2 interventions - of which ViSiGi® 3D suction calibration device is the first listed.
NCT03939819 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03939819 about?
NCT03939819 is a clinical study titled "Endoscopic vs. Suction Device Calibration in Sleeve Gastrectomy". This study aims to compare the difference in staple usage and post-operative GERD (heartburn) between patients that had an endoscope used versus patients that had a suction calibration system used on them during "laparoscopic sleeve gastrectomy" (LSG).
What is the current status of trial NCT03939819?
This trial is currently completed. It is a NA study. The enrollment target is 106 participants. The study started on 2019-07-30. Estimated completion is 2022-02-02.
What interventions are being tested in trial NCT03939819?
The interventions under investigation include: ViSiGi® 3D suction calibration device (DEVICE), Esophagogastroduodenoscopy (EGD) calibration (DEVICE).
Who is sponsoring clinical trial NCT03939819?
This trial is sponsored by Emory University, which has 1,208 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03939819's enrollment target sits among peer trials
106 830th of 2000 higher than 1,167 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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