CLINICAL_TRIALS
ClinicalTrials.gov record update
A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase Ⅲ, Efficacy and Safety Study of INTRAROSA® (Prasterone) Vaginal Inserts on Postmenopausal Vulvovaginal Atrophy (VVA)
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT04982692
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-25T22:26:06.550087+00:00
- Published At
- 2024-10-18T00:00:00+00:00
- Record Updated At
- 2024-10-18
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Postmenopausal Vulvovaginal Atrophy"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-10-18"- protocolSection.identificationModule.nctId
"NCT04982692"- protocolSection.identificationModule.officialTitle
"A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Group, Phase \u2162, Efficacy and Safety Study of INTRAROSA\u00ae (Prasterone) Vaginal Inserts on Postmenopausal Vulvovaginal Atrophy (VVA)"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["PHASE3"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.