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NCT06953635 · ClinicalTrials.gov registry record · NA
Quadratus Lumborum Versus Placebo in Open Ventral Hernia Repair
A NA study, sponsored by University of Tennessee Graduate School of Medicine.
- Not yet
- Registry status
- NA
- Development phase
- 70
- Enrollment target
NCT06953635 is a NA study that has not yet begun recruiting, run by University of Tennessee Graduate School of Medicine. The registered enrollment target is 70 participants.
The verdict
NCT06953635, a NA study, has not yet begun recruiting, sponsored by University of Tennessee Graduate School of Medicine.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 70 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether using a QL block is better than placebo (a look-alike substance that contains no drug) in lowering the amount of opioids you need for pain relief in the first 24 hours and if it improves your recovery following a ventral hernia repair. Participants will be asked to complete a questionnaire before surgery and again at their 30-day follow up. You will also be asked to complete a pain diary 24 hours after surgery and attend a follow-up visit approximately 30 days after surgery. The following information will be collected from you or your medical record: 1. Pain medications given to you during surgery. 2. Pain medications prescribed to you after surgery, including medication name, dose, units, and frequency. 3. Pain levels during the first 24 hours after surgery. 4. Your total hospital length of stay after surgery. 5. Any complications that you may have experienced after surgery. 6. Demographic information, medical history as well as details about your hernia repair surgery.
Interventions
- PROCEDURE Placebo
- PROCEDURE Quadratus Lumborum (QL) Block
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70 participants |
| Start Date | 2025-06-01 |
| Est. Completion | 2026-02-28 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06953635
The ClinicalTrials.gov registry entry for NCT06953635 describes a study currently listed as not yet recruiting, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Tennessee Graduate School of Medicine, which has 20 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT06953635 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06953635 about?
NCT06953635 is a clinical study titled "Quadratus Lumborum Versus Placebo in Open Ventral Hernia Repair". The purpose of this study is to determine whether using a QL block is better than placebo (a look-alike substance that contains no drug) in lowering the amount of opioids you need for pain relief in the first 24 hours and if it improves your recovery following a ventral hernia repair. Participants ...
What is the current status of trial NCT06953635?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2025-06-01. Estimated completion is 2026-02-28.
What interventions are being tested in trial NCT06953635?
The interventions under investigation include: Placebo (PROCEDURE), Quadratus Lumborum (QL) Block (PROCEDURE).
Who is sponsoring clinical trial NCT06953635?
This trial is sponsored by University of Tennessee Graduate School of Medicine, which has 20 total clinical trials registered on ClinicalTrials.gov.
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