Status:
UNKNOWN
Rectal Acetaminophen During Oocyte Retrievals
Lead Sponsor:
University of South Florida
Conditions:
Oocyte Retrieival and Post Operative Pain Control
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
As the opioid epidemic shows no sign of abating, this national crisis deserves careful attention from all medical subspecialties. This includes reproductive endocrinology and infertility (REI), where ...
Detailed Description
There are various methods of anesthesia used for transvaginal ultrasound guided oocyte retrievals. The majority of cases are performed under conscious sedation with a combination of sedative-hypnotic ...
Eligibility Criteria
Inclusion
- Any female patient undergoing oocyte retrieval by transvaginal ultrasound-guided ovarian puncture.
- \-
Exclusion
- Patients with chronic pain conditions such as fibromyalgia and sickle cell anemia.
- Patient with BMI greater than 40
- Patients undergoing transabdominal ultrasound guided oocyte retrieval
- Patients that required general endotracheal intubation anesthesia in prior oocyte retrieval.
- Patients with documented allergic reaction to acetaminophen or oxycodone
- 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.
- Patients who develop complication such as PID post procedure.
- \-
Key Trial Info
Start Date :
August 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 1 2025
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT05990868
Start Date
August 1 2023
End Date
August 1 2025
Last Update
August 14 2023
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