the Effect of Pre-sacral Nerve Block on Post-operative Pain Following Laparoscopic Hysterectomy
Gynecology
About this trial
This is an interventional prevention trial for Gynecology
Eligibility Criteria
Inclusion Criteria: Women undergoing elective total laparoscopic hysterectomy Body mass index less than 29 Kg/m2 Exclusion Criteria: Previous presacral neurectomy Concurrent surgical procedure other than salpingectomy and/or oophorectomy Chronic narcotic consumption Inability to provide consent Patients with contraindication to laparoscopic surgery (e.g. severe cardiopulmonary dysfunction). Bleeding tendency (e.g. patient on anticoagulants, platelets disorders) Intra-abdominal adhesions (due to previous abdominal surgery e.g. myomectomy)
Sites / Locations
- Ain Shams universityRecruiting
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Placebo
pre-sacral nerve block
Before the removal of uterus and the closure of vaginal cuff, insertion of 6inch 22G needle 2 to 3 cm below the umbilicus, 30 ml normal saline (sodium chloride solution 0.9%, FIPCO, Egypt)will be administered , then the uterus will be removed, and the operation will be terminated
Uterosacral nerve block will be performed before the removal of uterus and the closure of vaginal cuff, and before the removal of trocars from abdominal cavity, insertion of 6-inch 22G needle 2 to 3 cm below the umbilicus, injection of the SHP area which situated anterior to L5-S1 vertebral bodies, Caudal to the bifurcation of the abdominal aorta with 30 ml 0.25% bupivacaine (Marcaine®0.25% , Astra Zeneca, Egypt) will be administered. Following the injection of local anesthetic, patient will be placed from Trendelenburg position to horizontal position. The we will remove the uterus and trocars , and the operation will be terminated. Data will be recorded in a case report form (CRF) and statistical analysis will be done.