Status:
COMPLETED
An Investigational Drug Study in the Treatment of Primary Dysmenorrhea (0663-064)
Lead Sponsor:
Organon and Co
Conditions:
Dysmenorrhea
Eligibility:
FEMALE
18+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to evaluate the pain relieving effect and safety of an investigational drug in women with moderate to severe primary dysmenorrhea (painful menstruation).
Eligibility Criteria
Inclusion
- Women 18 years of age or older suffering from painful menstruation
Exclusion
- Women taking medications that are not allowed in the study (such as pain medications, antidepressants, tranquilizers, hypnotics, sedatives, or oral contraceptives).
- Women who are pregnant, breast-feeding or within 6 weeks of giving birth
Key Trial Info
Start Date :
June 7 2002
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 6 2002
Estimated Enrollment :
129 Patients enrolled
Trial Details
Trial ID
NCT00092729
Start Date
June 7 2002
End Date
December 6 2002
Last Update
August 15 2024
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