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NCT07153614 · ClinicalTrials.gov registry record · NA
Efficacy of Perioperative Opioid Sparing Techniques on Time to Initiation of Chemotherapy
A NA study of Perioperative Opioid Sparing Techniques, sponsored by University of Tennessee Graduate School of Medicine.
- Recruiting
- Registry status
- NA
- Development phase
- 200
- Enrollment target
- 1
- Study location
NCT07153614 is a NA study of Perioperative Opioid Sparing Techniques that is actively recruiting participants, run by University of Tennessee Graduate School of Medicine. The registered enrollment target is 200 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07153614, a NA study of Perioperative Opioid Sparing Techniques, is actively recruiting participants, sponsored by University of Tennessee Graduate School of Medicine.
- RECRUITING
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary purpose of this study is to determine if intrathecal morphine (ITM) administration is superior to quadratus lumborum block or surgeon administered transversus abdominis plane (TAP) blocks result in decreased time to initiation of chemotherapy following oncologic surgery. The secondary objectives of this study are to determine: * The difference between interventions in time to return of bowel function in days * The difference between interventions in incidence of opioid related adverse drug events (ORADEs) * The difference between interventions in cumulative and post-operative total morphine milligram equivalents * The difference between interventions in quality-of-life assessment tool and patient satisfaction (brief pain index short form BPI-sf9) * The difference between interventions in hospital length of stay in days * The difference between cumulative pain scores between interventions * The difference between short acting and long-acting bupivacaine in pain management and time to chemotherapy The hypothesis is that preoperative intrathecal morphine administration will significantly reduce the time to initiation of postoperative chemotherapy.
Conditions Studied
Interventions
- PROCEDURE Intrathecal Morphine Block
- PROCEDURE Bilateral Quadratus Lumborum Block
- PROCEDURE Bilateral Transverse Abdominis Plane Block
Study Locations (1)
Tennessee
- University of Tennessee Graduate School of Medicine - Knoxville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2025-02-03 |
| Est. Completion | 2027-02-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07153614
The ClinicalTrials.gov registry entry for NCT07153614 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 200 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 1 condition, with Perioperative Opioid Sparing Techniques appearing as the primary indexed condition, and to 3 interventions - of which Intrathecal Morphine Block is the first listed.
NCT07153614 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT07153614 about?
NCT07153614 is a clinical study titled "Efficacy of Perioperative Opioid Sparing Techniques on Time to Initiation of Chemotherapy". The primary purpose of this study is to determine if intrathecal morphine (ITM) administration is superior to quadratus lumborum block or surgeon administered transversus abdominis plane (TAP) blocks result in decreased time to initiation of chemotherapy following oncologic surgery. The secondary o...
What is the current status of trial NCT07153614?
This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2025-02-03. Estimated completion is 2027-02-03.
What conditions does trial NCT07153614 study?
This clinical trial studies the following conditions: Perioperative Opioid Sparing Techniques.
What interventions are being tested in trial NCT07153614?
The interventions under investigation include: Intrathecal Morphine Block (PROCEDURE), Bilateral Quadratus Lumborum Block (PROCEDURE), Bilateral Transverse Abdominis Plane Block (PROCEDURE).
Who is sponsoring clinical trial NCT07153614?
This trial is sponsored by University of Tennessee Graduate School of Medicine, which has 20 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07153614 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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