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NCT06508814 · ClinicalTrials.gov registry record · NA
Pain With Differing Insufflation Pressures During Laparoscopic Hysterectomy
A NA study of Postoperative Pain, sponsored by University of Tennessee.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT06508814: Recruiting NA study of Postoperative Pain, sponsored by University of Tennessee.
NCT06508814 is a NA study of Postoperative Pain that is actively recruiting participants, run by University of Tennessee. The registered enrollment target is 100 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06508814, a NA study of Postoperative 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 |
What NCT06508814 shows while recruiting
NCT06508814 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (57% lower).
The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Lower Insufflation Pressure is the first listed.
NCT06508814 reports a single indexed study location in 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: Postoperative 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
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06508814's enrollment target sits among peer trials
100 55th of 120 higher than 59 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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