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Clinical Trial Summary

The main objective of the study is the comparison of the effective duration of hospitalization following laparoscopic hysterectomy via a single-port peri-umbilical technique versus an conventional multi-port technique.


Clinical Trial Description

The secondary objectives are to compare the following between the two arms of the study:

1. the difference between the real discharge date and the theoretical discharge date

2. measures related to intraoperative bleeding

3. operating time

4. postoperative pain

5. quality of life

6. abdominal wall complication rates

7. rates of further surgery and rehospitalization

8. use of material resources in the operating room

9. average costs of hospital stay

10. Costs of rehospitalization at 1 year

11. Indirect costs ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01830738
Study type Interventional
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Terminated
Phase N/A
Start date February 2014
Completion date April 2015

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