Randomized controlled trial of efficacy and safety of pre-operative GnRH agonist administration for laparoscopic myomectomy.
Not Applicable
- Conditions
- uterine fibroid
- Registration Number
- JPRN-UMIN000000879
- Lead Sponsor
- Dept. of OB/GY Juntendo univ. school of medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with a history of hypersensitivity to ingerdients of the investigational drug or to any synthetic LH-RH agent or LH-RH derivative Women sho are or potentially may be pregnant Lactating women Women with non-diagnosable, abnormal bleedng of unknown origin
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rate of myomas at 6 months after GnRHa administration. The side effects during GnRHa administration. The estimated bleeding during operation, duration of operation and the weight of extracted specimens.
- Secondary Outcome Measures
Name Time Method The recurrence rate evaluated by MRI after LM. Pregnancy outcome after LM.