The goal of this clinical trial is to compare the laparoscopic and transvaginal closure techniques of the vaginal vault in patients who perform TLH, regarding the risk of vaginal vault hematoma and other complications as vaginal cuff infection and sexual dysfunction.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Enrollment
48
Removal of uterus and cervix by laparoscope
Ain Shams University maternity hospital
Cairo, Egypt
RECRUITINGVaginal Vault hematoma
It will be assessed by examination and ultrasound
Time frame: From 10 days postoperative to 30 days postoperative
Bleeding/spotting
I wil be assed by history and examination
Time frame: From 10 days postoperative to 30 days postoperative
Vaginal infection:
It will be assessed by history and examination
Time frame: From 10 days postoperative to 30 days postoperative
Vaginal prolapse
It will be assessed by history and examination
Time frame: From 10 days postoperative to 30 days postoperative
Vaginal cuff granulation
It will be assessed by examination and ultrasound
Time frame: From 10 days postoperative to 30 days postoperative
Sexual dysfunction
I will be assessed through Female Sexual Function Index (FSFI) questionnaire
Time frame: From 3 to 4 months post operative
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