Status:
COMPLETED
Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery
Lead Sponsor:
Scripps Health
Conditions:
Post-operative Pain
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasiv...
Detailed Description
Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasiv...
Eligibility Criteria
Inclusion
- Patients 18 years of age or older scheduled to undergo robotic-assisted laparoscopic hysterectomy for benign conditions.
Exclusion
- Known or suspected malignancy,
- Active liver/renal disease,
- Chronic alcohol use/alcoholism,
- Allergy to acetaminophen,
- Conversion to laparotomy,
- hx gastroparesis,
- Poorly controlled insulin dependent diabetes or gastric bypass surgery,
- Regular/recent (past 6 months) narcotic use,
- Inability to swallow pills.
Key Trial Info
Start Date :
February 1 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2018
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT03391284
Start Date
February 1 2016
End Date
February 1 2018
Last Update
November 22 2022
Active Locations (2)
Enter a location and click search to find clinical trials sorted by distance.
1
Scripps Clinic
San Diego, California, United States, 92130
2
Scripps Clininc Dept of Ob/Gyn
San Diego, California, United States, 92130