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A Randomized Parallel Group Controlled Study between 3.75 mg of Leuprorelin and 1.8 mg of Goserelin Depot in the Sequential Therapy (GnRH Agonist + Dienogest) for Treatment of Endometriosis

Phase 4
Recruiting
Conditions
endometriosis, chocolate cyst or adenomyosis uteri
Registration Number
JPRN-UMIN000010332
Lead Sponsor
Tokyo Women's Medical University Department of Obstetrics and Gynecology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
120
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients with undiagnosed abnormal genital bleeding 2. Pregnant or possibly pregnant women 3. Lactating patients 4. Patients with a past history of hypersensitivity to GnRH agonists or dienogest 5. Patients treated with hormone drugs (oral contraceptive, danazol, GnRH agonists, etc.) and dienogest within the past 4 months 6. Other patients considered ineligible as subjects by investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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