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NCT02628093 · ClinicalTrials.gov registry record · NA
A ProspectiveTrial Comparing THUNDERBEAT to the Ligasure Energy Device During Laparoscopic Colon Surgery
A NA study, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- NA
- Development phase
- 73
- Enrollment target
NCT02628093 is a NA study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 73 participants.
The verdict
NCT02628093, a NA study, has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- NA
- Development phase
- 73 participants
- Enrollment target
Study Summary
Prospective randomized controlled study, at Colon and Rectal Surgery, WMC/NYPH. Subjects undergoing Laparoscopic Left Colectomy will be randomized into 1 of 2 groups based on the instrument used for tissue dissection and vessel ligation: Group 1 - THUNDERBEAT Group 2 \- Ligasure Population
Interventions
- DEVICE LIGASURE
- DEVICE THUNDERBEAT
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 73 participants |
| Start Date | 2016-02-17 |
| Est. Completion | 2019-05-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02628093
The ClinicalTrials.gov registry entry for NCT02628093 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 73 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which LIGASURE is the first listed.
NCT02628093 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02628093 about?
NCT02628093 is a clinical study titled "A ProspectiveTrial Comparing THUNDERBEAT to the Ligasure Energy Device During Laparoscopic Colon Surgery". Prospective randomized controlled study, at Colon and Rectal Surgery, WMC/NYPH. Subjects undergoing Laparoscopic Left Colectomy will be randomized into 1 of 2 groups based on the instrument used for tissue dissection and vessel ligation: Group 1 - THUNDERBEAT Group 2 \- Ligasure Population
What is the current status of trial NCT02628093?
This trial is currently completed. It is a NA study. The enrollment target is 73 participants. The study started on 2016-02-17. Estimated completion is 2019-05-02.
What interventions are being tested in trial NCT02628093?
The interventions under investigation include: LIGASURE (DEVICE), THUNDERBEAT (DEVICE).
Who is sponsoring clinical trial NCT02628093?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
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