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Not Yet Recruiting
NCT07664956
Cyclobenzaprine for Postoperative Pain in Minimally Invasive Hysterectomy
Conditions: Minimally Invasive Surgical Procedures, Abnormal Uterine Bleeding, Unspecified, Adenomyosis of Uterus, Fibroid Uterus, Chronic Pelvic Pain, Endometriosis, Menorrhagia, Endometritis, Adnexal Diseases
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 36
Sponsor: Christiana Care Health Services
Location: ChristianaCare Health System Newark Delaware
Summary
Typical postoperative pain control after minimally invasive hysterectomy includes ibuprofen, acetaminophen, and a short course of narcotics. The purpose of this study is to see if adding cyclobenzaprine to this regime improves pain control and lessens narcotic use.
Eligibility Criteria
Inclusion Criteria:
* Age \>18yo
* Female
* English speaking
* Undergoing (robotic assisted or classic) total laparoscopic hysterectomy ± unilateral or bilateral salpingectomy ± unilateral or bilateral oophorectomy
* If other procedures such as lysis of adhesions, excision of endometriosis, or ureterolysis are indicated based on intraoperative evaluation, those patients may still be included
* Surgery took place at ChristianaCare Hospitals
* No allergies or contraindications to standard of care post operative pain medications (acetaminophen, NSAIDs, narcotics) or cyclobenzaprine
Exclusion Criteria:
* Age \
Source: ClinicalTrials.gov (NCT07664956). StuddyBuddy aggregates publicly available trial information.