Rectal Acetaminophen Use During Oocyte Retrievals to Reduce Post-Operative Opioid Utilization
Stopped early · Phase 4
Conditions studied: Opioid Use
In brief
The primary aim of this study is to evaluate the administration of rectal acetaminophen to current and standard anesthesia and analgesia protocol in oocyte retrievals would reduce postoperative utilization of opioids (Tylenol with codeine) in fertility patients.
Key facts
- Study ID
- NCT03732469
- Run by
- University of South Florida
- People needed
- 4
- Starts
- 2019-11-01
- Expected to finish
- 2021-03-01
- Last updated by the study team
- 2021-06-18
Who can join
Age: 18 and older, up to 56. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Any female patient undergoing oocyte retrieval by transvaginal ultrasound-guided ovarian puncture
You may not qualify if…
- Patients with chronic pain conditions such as fibromyalgia and sickle cell anemia.
- Patient with BMI greater than 40
- Patients that required general endotracheal intubation anesthesia in prior oocyte retrieval
- Patients with documented allergic reaction to acetaminophen
- Patient with contra-indication to the use of acetaminophen (liver disease)
- Patients with a history of past or current alcohol, drug or opioid abuse
- Patients with ulcerative colitis, Crohn's disease, or severe rectal hemorrhoids
Where it is running
- University of South Florida — Tampa, Florida, United States
Full record on ClinicalTrials.gov
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