Post Operative Pain Clinical Trial
Official title:
A Randomized, Controlled, Observer-blinded Pilot Trial of Laparoscopic Large Volume, Multisite Transversus Abdominal Plane (TAP) Block With Liposomal Bupivacaine in Patients Undergoing Minimally Invasive Hysterectomy for Endometrial Cancer
Verified date | January 2024 |
Source | Tufts Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Modern postoperative pain management aims to optimizing pain relief while minimizing opiate usage. While opiates are effective for pain relief, they result in common adverse effects such as nausea, constipation, and urinary retention, and most importantly present a long-term risk of abuse and dependency. Commonly used approaches include non-opiate pain medications such as acetominophen and non-steroidal anti-inflammatory agents, as well as regional nerve blocks such as epidurals. The transversus abdominis plane (TAP) block is a fascial plane block performed by injecting local anesthetic into the plane superficial to the transversus abdominis muscle where the anterior rami of the spinal nerves course to provide sensory innervation to the abdominal wall. The injections are generally placed either subcostally or at the midaxillary line bilaterally. The TAP block has been shown to be effective in reducing pain scores and opiate usage in some randomized studies but not others in patients undergoing various abdominal surgeries. There is great variation in method of administration, sites injected, and local anesthetics used, which may in part account for the heterogeneity of trial results.
Status | Enrolling by invitation |
Enrollment | 15 |
Est. completion date | September 30, 2024 |
Est. primary completion date | June 30, 2024 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: 1. Age 18-80 2. Patients undergoing laparoscopic or robotic hysterectomy; may include other procedures (e.g. lymph node removal) 3. Endometrial cancer or endometrial intraepithelial neoplasia 4. Able to consent to study Exclusion Criteria: 1. Known clinically significant allergy to bupivacaine or liposomal bupivacaine 2. ASA IV or V 3. Emergency surgery 4. Current chronic opiate use 5. Current pregnancy or breastfeeding 6. Severe hepatic or renal impairment 7. Hysterectomy is not for endometrial cancer or endometrial intraepithelial neoplasia |
Country | Name | City | State |
---|---|---|---|
United States | Tufts Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Tufts Medical Center |
United States,
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* Note: There are 30 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduced opiate use in both TAP block arms. | Demonstrate a statistically significant change in postoperative opiate use as measured in oral morphine milligram equivalents on postoperative days 0-7. | 7 days | |
Secondary | Increase in opiate-free participants by day 7 | Demonstrate a change in proportion of subjects that are opiate-free on postoperative days 0-7. | 7 days | |
Secondary | Reduction in post-operative resting pain scores | Demonstrate a statistically significant change in maximum resting numeric rating scale (NRS) at the following time points in postoperative days: 0-1, 1-2, 2-3, 0-7. | 7 days | |
Secondary | Improvement in patient satisfaction regarding pain control | Demonstrate change in patient satisfaction with regard to pain control (very satisfied, satisfied, unsatisfied). | 7 days | |
Secondary | Incidence of Treatment-Emergent Adverse Events | Specific AEs measured will be nausea, headache, rash, itching, hematoma, ecchymosis, seizures | 7 days |
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