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NCT06305975 · ClinicalTrials.gov registry record · NA
Blunt Fascial vs. Veress Needle Peritoneal Entry in Laparoscopic Gynecologic Surgery
A NA study of Laparoscopic Surgery, sponsored by Cedars-Sinai Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT06305975 is a NA study of Laparoscopic Surgery that is actively recruiting participants, run by Cedars-Sinai Medical Center. The registered enrollment target is 100 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06305975, a NA study of Laparoscopic Surgery, is actively recruiting participants, sponsored by Cedars-Sinai Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
This study aims to investigate the effect of two peritoneal entry techniques on intraoperative and post-operative outcomes among patients undergoing laparoscopic surgery with a minimally invasive gynecologic surgeon. Patients will be randomized to either blunt fascial or veress needle peritoneal entry. Insufflation times, failed entries, complications and post-operative pain scores will be collected. The investigators hypothesize that the blunt entry technique will be associated with shorter insufflation times and similar intraoperative and postoperative outcomes compared with the veress needle entry technique. Primary Objective: To evaluate the insufflation times and success upon peritoneal entry according to peritoneal entry technique. Secondary Objectives: To evaluate the surgical outcomes and patients pain scores according to peritoneal entry technique.
Conditions Studied
Interventions
- PROCEDURE Blunt fascial abdominal entry
- PROCEDURE Veress needle abdominal entry
Study Locations (1)
California
- Cedars Sinai Medical Center - Los Angeles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-03-22 |
| Est. Completion | 2025-03-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06305975
The ClinicalTrials.gov registry entry for NCT06305975 describes a study currently listed as recruiting, 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 Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Laparoscopic Surgery appearing as the primary indexed condition, and to 2 interventions - of which Blunt fascial abdominal entry is the first listed.
NCT06305975 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT06305975 about?
NCT06305975 is a clinical study titled "Blunt Fascial vs. Veress Needle Peritoneal Entry in Laparoscopic Gynecologic Surgery". This study aims to investigate the effect of two peritoneal entry techniques on intraoperative and post-operative outcomes among patients undergoing laparoscopic surgery with a minimally invasive gynecologic surgeon. Patients will be randomized to either blunt fascial or veress needle peritoneal ent...
What is the current status of trial NCT06305975?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-03-22. Estimated completion is 2025-03-01.
What conditions does trial NCT06305975 study?
This clinical trial studies the following conditions: Laparoscopic Surgery.
What interventions are being tested in trial NCT06305975?
The interventions under investigation include: Blunt fascial abdominal entry (PROCEDURE), Veress needle abdominal entry (PROCEDURE).
Who is sponsoring clinical trial NCT06305975?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06305975 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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