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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02591251
Other study ID # VCL
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date October 2015
Est. completion date March 2016

Study information

Verified date August 2022
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Laparoscopy is a minimally invasive method used for diagnostic and therapeutic purposes. It allows surgeons to take a look on the abdominal and pelvic organs. Diagnostic laparoscopy is usually done in an operating room under general anesthesia. The procedure takes about 25 minutes and the patients usually discharged in the same day. The laparoscopy can diagnose pelvic pathological conditions in approximately 50% of the cases. However, the laparoscopy has some complications, such as infections, hemorrhage and injuries of visceral organs. A preoperative vaginal preparation is important to prevent the bacteria colonization in a trial to avoid postoperative infection after laparoscopic surgery. The povidone-iodine (PI) is normally used as a skin and vaginal disinfectant to prevent postoperative infections, however; it can be the cause of significant postoperative irritation. There are many reports in the literature proved that the mechanical cleansing of the vagina, not the use of an antiseptic solution, is responsible for the efficacy of vaginal preparations. In the field of assisted reproductive technology; A study in 1992 concluded that the infection rates with normal saline solution are comparable to PI. Another proved that, a normal saline solution can be effective in prevention of preventing postoperative infections after vaginal surgery. The most recent study by Lewis et al has been shown that the Baby shampoo is preferable than PI in vaginal cleansing before gynecologic procedures because it has minimal vaginal irritation and cheaper than PI. So the optimal vaginal antiseptic solution is unknown, the investigators want to conduct a randomized trial comparing 2 commonly used vaginal antiseptic solutions: PI and the saline solution before the laparoscopic surgery. The normal saline is used in medicine as an intravenous isotonic infusion and for cleaning wounds. It is a mild but effective cleaning agent and will not harm normal tissue, unlike many stronger antiseptics. It is available and inexpensive in comparison to povidone iodine.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: 1 - All women who will subject to laparoscopy (diagnostic or operative) for gynecological problems Exclusion Criteria: 1 - All women who will subjected to operative laparoscopy for myomectomy or hysterectomy. 2- All patients have current vaginitis or urinary tract infection before the laparoscopy. 3- Diabetic women. 4- Women with BMI > 25 kg/m2.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Povidone-iodine solution

Normal saline solution


Locations

Country Name City State
Egypt Assiut university Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Degree of fever postoperative (c) 1 month
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