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NCT05692986
Chlorhexidine vs Povidone Iodine Vaginal Prep in Decreasing Postoperative Infection in Total Laparoscopic Hysterectomy
Conditions: Preventative Laparoscopic Hysterectomy
Sex: Female
Healthy volunteers: 1
Phase: NA
Sponsor: Henry Ford Health System
Summary
This is a randomized control trial which will randomize patients who will be undergoing laparoscopic (conventional or robotic assisted) total hysterectomy to vaginal prep with 4% chlorhexidine gluconate vs 10% povidone iodine.
There is paucity of information regarding the superiority of one over the other.
Eligibility Criteria
Inclusion Criteria:Patients who are scheduled for total laparoscopic hysterectomyExclusion Criteria:not able to consent in English or have allergy to the 10% povidone betadine or 4% chlorhexidine solution.
Source: ClinicalTrials.gov (NCT05692986). StuddyBuddy aggregates publicly available trial information.