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CLINICAL_TRIALS ClinicalTrials.gov record update

The Optimum Dose of Vaginal Misoprostol Prior to Office Hysteroscopy: Double Blind Randomized Controlled Trial

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT01612065
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:35:31.496054+00:00
Published At
2013-04-11T00:00:00+00:00
Record Updated At
2013-04-11
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
["Infertility", "Abnormal Uterine and Vaginal Bleeding, Unspecified", "Recurrent Abortion"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2013-04-11"
protocolSection.identificationModule.nctId
"NCT01612065"
protocolSection.identificationModule.officialTitle
"The Optimum Dose of Vaginal Misoprostol Prior to Office Hysteroscopy: Double Blind Randomized Controlled Trial"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Infertility (protocolSection.conditionsModule.conditions)
  • Abnormal Uterine and Vaginal Bleeding, Unspecified (protocolSection.conditionsModule.conditions)
  • Recurrent Abortion (protocolSection.conditionsModule.conditions)

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.