Study for the Evaluation of the Efficiency of a Device for the Diagnosis of an Internal Rectal Prolapse, a Pelvic Floor Ptosis and for the Determination of an Internal Hernia Into the Douglas Pouch

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT00836680

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-28T10:34:56.864291+00:00

Published At

2009-02-04T00:00:00+00:00

Record Updated At

2009-02-04

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

["Internal Rectal Prolapse", "Pelvic Floor Ptosis", "Internal Hernia Into the Douglas Pouch"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2009-02-04"

protocolSection.identificationModule.nctId

"NCT00836680"

protocolSection.identificationModule.officialTitle

"Study for the Evaluation of the Efficiency of a Device for the Diagnosis of an Internal Rectal Prolapse, a Pelvic Floor Ptosis and for the Determination of an Internal Hernia Into the Douglas Pouch"

protocolSection.statusModule.overallStatus

"UNKNOWN"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Internal Rectal Prolapse (protocolSection.conditionsModule.conditions)
• Pelvic Floor Ptosis (protocolSection.conditionsModule.conditions)
• Internal Hernia Into the Douglas Pouch (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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