Contraception Clinical Trial
Official title:
Multi-Center, Randomized, Double-Blind Active-Controlled, Parallel Group Study to Investigate Plasma Folate, Red Blood Cell Folate and Homocysteine Levels During a 24 Week Oral Administration of an OC Containing Folate Compared to OC Alone
The purpose of this study is to determine whether the study drug is safe and effective
Acronym is used in result section: suspected/diagnosed (susp/diag) ;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
Status | Clinical Trial | Phase | |
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Completed |
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Completed |
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||
Completed |
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Active, not recruiting |
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N/A | |
Enrolling by invitation |
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Recruiting |
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Phase 2 | |
Completed |
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Completed |
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Withdrawn |
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N/A | |
Completed |
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Phase 1/Phase 2 | |
Completed |
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Phase 1 | |
Completed |
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N/A | |
Recruiting |
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Terminated |
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Recruiting |
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N/A | |
Withdrawn |
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N/A |