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NCT06508814 · ClinicalTrials.gov registry record · NA
Pain With Differing Insufflation Pressures During Laparoscopic Hysterectomy
A NA study of Post Operative Pain, sponsored by University of Tennessee.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT06508814 is a NA study of Post Operative Pain that is actively recruiting participants, run by University of Tennessee. The registered enrollment target is 100 participants, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06508814, a NA study of Post Operative Pain, is actively recruiting participants, sponsored by University of Tennessee.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the effect of decreased insufflation pressure on postoperative pain, analgesic use, and surgical safety and feasibility for laparoscopic hysterectomy.
Conditions Studied
Interventions
- PROCEDURE Lower Insufflation Pressure
- PROCEDURE Standard Insufflation Pressure
Study Locations (1)
Tennessee
- University of Tennessee Health Science Center - Memphis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-06-10 |
| Est. Completion | 2025-06-10 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06508814
The ClinicalTrials.gov registry entry for NCT06508814 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, below the 235-participant average among 56 other Post Operative Pain trials with a reported enrollment target (57% lower). The listed sponsor is University of Tennessee, which has 96 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Post Operative Pain appearing as the primary indexed condition, and to 2 interventions - of which Lower Insufflation Pressure is the first listed.
NCT06508814 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT06508814 about?
NCT06508814 is a clinical study titled "Pain With Differing Insufflation Pressures During Laparoscopic Hysterectomy". The purpose of this study is to determine the effect of decreased insufflation pressure on postoperative pain, analgesic use, and surgical safety and feasibility for laparoscopic hysterectomy.
What is the current status of trial NCT06508814?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-06-10. Estimated completion is 2025-06-10.
What conditions does trial NCT06508814 study?
This clinical trial studies the following conditions: Post Operative Pain.
What interventions are being tested in trial NCT06508814?
The interventions under investigation include: Lower Insufflation Pressure (PROCEDURE), Standard Insufflation Pressure (PROCEDURE).
Who is sponsoring clinical trial NCT06508814?
This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06508814 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
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