The comparison of surgical outcomes of using LigaSure and Gyrus PK in total laparoscopic hysterectomy

Not Applicable

• Conditions: laparoscopic hysterectomy; Surgery - Surgical techniques

• Registration Number: ACTRN12615000649516
• Lead Sponsor: Sydney West Advanced Pelvic Surgery Unit

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-06-23
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: Female
• Target Recruitment: 64

Inclusion Criteria

Patients requiring hysterectomy for benign indications as determined jointly by the surgeon and the patient;Non-pregnant female patients;Over 35 years of age at time of surgery;Patients with the following (but not limited to) diagnoses: abnormal uterine bleeding, fibroids, prolapse;Patients who understand the conditions of the study and are willing to participate for the length of the prescribed term of follow-up; Patients who are capable of, and have given, informed consent to their participation in the study.

Exclusion Criteria

Pregnancy or malignancy suspected ;Uterus exceeding 14 weeks in size

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
operative time (from skin incision to detachment of the uterus with secured haemostasis)[during surgery]

Secondary Outcome Measures

Name	Time	Method
intra-operative blood loss (Intra-operative blood loss is calculated by subtracting the total volume of irrigation fluid being used from the total volume of fluid in the suction bottle.)[at completion of surgery];major complications-review operation reports[during surgery];post-operative analgesics usage-<br>review medication charts[day 1 post-operation<br>];conversion rate-review operation report[during surgery];ergonomics<br>-use questionnarie that specially designed for this study[during surgery];cost-calculate disposable items on the count sheet [during surgery]