aparoscopic hysterectomy with 3,5mm instruments

Not Applicable

• Conditions: N92.0; Leiomyoma of uterus, unspecified; Excessive and frequent menstruation with regular cycle; D25.9

• Registration Number: DRKS00003635
• Lead Sponsor: niversitätsklinikum Mannheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-04-04
• Study Completion: 2013-05-17
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 31

Inclusion Criteria

Indication for laparoscopic hysterectomy

Exclusion Criteria

Patients who refuse to take part in the trial

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time needed for the operation with the smaller instruments. The time is electronically documented and will be requested after the operation.

Secondary Outcome Measures

Name	Time	Method
Bloodloss because of the smaller instruments. This will be checked by hemoglobin level within 24 hours after the operation and compared with the level before the operation. The 50 operated patients will be compared to 50 patients already operated with 5mm instruments.