NCT Number: NCT00244452
A Multinational, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Investigate the Efficacy, Safety and Duration of Effect of a Single Administration of Various Doses of Cetrorelix SR in Subjects With Histologically Confirmed Endometriosis
Identify effective doses of cetrorelix SR in the treatment of symptoms of endometriosis, describe dose effect relationship and duration of symptom relief
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Notify MeKey information
Conditions
Age range
18 year–45 year
Sex eligibility
Female
Study type
Interventional
Phase
Phase 2
Primary location
Site 6101, Clayton, Australia
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Premenopausal female,
- history of regular menstrual periods,
- any of the symptoms dysmenorrhea,
- dyspareunia or pelvic pain assessed as moderate to severe,
- endometriosis confirmed by histology within 36 months,
- use of barrier contraception throughout the study
Exclusion criteria
- Insufficient wash out period for other endometriosis treatments,
- resection or destruction of endometriotic lesions less than 12 weeks prior to screening,
- need for strong opioid analgesics,
- need for immediate surgical treatment of endometriosis,
- any condition that interferes with adherence to study procedures or study assessments
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Solvay Pharmaceuticals
Industry
Registry information
Important dates
- Study start
- 2005
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Oct 26, 2005
- Registry last updated
- Mar 31, 2008
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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