An exploratory study of NS-580 in patients with endometriosis (early phase II)
Phase 2
Completed
- Conditions
- endometriosis
- Registration Number
- JPRN-jRCT2080223592
- Lead Sponsor
- ippon Shinyaku Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- completed
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
Patients who have been clinically diagnosed with endometriosis
Exclusion Criteria
Patients for whom surgical treatment for an organic disease is judged by the principal (sub-) investigator to be a priority
Patients with ovarian endometriomas that are found to be containing solid components
Patients who may be taking analgesics regularly during the study period
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method efficacy<br>exploratory<br>The change in pain VAS score
- Secondary Outcome Measures
Name Time Method efficacy<br>exploratory<br>The change in EHP-30 score