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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 is a NA study that has completed, run by Emory University. The registered enrollment target is 106 participants.
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).
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03939819
The ClinicalTrials.gov registry entry for NCT03939819 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Emory University, which has 1,208 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which ViSiGi® 3D suction calibration device is the first listed.
NCT03939819 reports 0 study locations.
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.
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