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NCT02896036 · ClinicalTrials.gov registry record · NA
Veress Entry With/Without Concomitant CO2
A NA study, sponsored by University of South Florida.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT02896036 is a NA study that has completed, run by University of South Florida. The registered enrollment target is 100 participants.
The verdict
NCT02896036, a NA study, has completed, sponsored by University of South Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study Summary
Purpose: The primary objective is to compare the time required for adequate intraperitoneal insufflation (from skin incision to reaching intraperitoneal pressure of 15 mmHg). Also the number of attempts needed before successful entry is achieved. The secondary objectives will evaluate rates of secondary outcomes measures such as; failed entry, extra peritoneal insufflation, vascular injury, visceral injury, gas embolism, solid organ injury, and omental injury between the two techniques. Study design: prospective randomized control trial Hypothesis: The investigators hypothesize that participant's undergoing laparoscopic surgery for benign Gynecologic indications at TGH who undergo laparoscopic entry technique of Veress needle entry with concomitant CO2 insufflation will require less time to achieve a 15 mmHg of intraperitoneal pressure as opposed to Veress needle entry with subsequent CO2 insufflation, and will require less number of attempts to achieve successful entry.
Interventions
- PROCEDURE Veress needle entry with concomitant CO2
- PROCEDURE Veress needle entry with subsequent CO2
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2016-08 |
| Est. Completion | 2018-03-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02896036
The ClinicalTrials.gov registry entry for NCT02896036 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of South Florida, which has 252 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Veress needle entry with concomitant CO2 is the first listed.
NCT02896036 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02896036 about?
NCT02896036 is a clinical study titled "Veress Entry With/Without Concomitant CO2". Purpose: The primary objective is to compare the time required for adequate intraperitoneal insufflation (from skin incision to reaching intraperitoneal pressure of 15 mmHg). Also the number of attempts needed before successful entry is achieved. The secondary objectives will evaluate rates of secon...
What is the current status of trial NCT02896036?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2016-08. Estimated completion is 2018-03-10.
What interventions are being tested in trial NCT02896036?
The interventions under investigation include: Veress needle entry with concomitant CO2 (PROCEDURE), Veress needle entry with subsequent CO2 (PROCEDURE).
Who is sponsoring clinical trial NCT02896036?
This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.
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