Last updated: July 31, 2024
Sponsor: University of Tennessee
Overall Status: Active - Recruiting
Phase
N/A
Condition
Post-surgical Pain
Acute Pain
Pain
Treatment
5x Oxycodone Oral Tablets
16x Oxycodone Oral Tablets
Clinical Study ID
NCT06532708
24-09978-FB
Ages 18-80 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Women aged 18 to 80
Undergoing planned laparoscopic hysterectomy as a day surgery procedure
Exclusion
Exclusion Criteria:
Women aged 18 to 80
Undergoing a non-laparoscopic unplanned surgical procedure
Patients with a history of opioid use disorder or current opioid use disorder
Study Design
Total Participants: 12
Treatment Group(s): 2
Primary Treatment: 5x Oxycodone Oral Tablets
Phase:
Study Start date:
July 12, 2024
Estimated Completion Date:
October 31, 2024
Study Description
Connect with a study center
University of Tennessee Health Science Center
Memphis, Tennessee 38103
United StatesActive - Recruiting
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