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CLINICAL_TRIALS ClinicalTrials.gov record update

Mesh Augmented Reinforcement of Abdominal Wall Suture Line in Patients Undergoing Midline Laparotomy to Limit the Rate of Incisional Hernia Occurrence

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
NCT05424484
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:28:57.377736+00:00
Published At
2025-11-19T00:00:00+00:00
Record Updated At
2025-11-19
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
["Incisional Hernia", "Incisional Hernia of Midline of Abdomen", "Midline Laparotomy"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-11-19"
protocolSection.identificationModule.nctId
"NCT05424484"
protocolSection.identificationModule.officialTitle
"Mesh Augmented Reinforcement of Abdominal Wall Suture Line in Patients Undergoing Midline Laparotomy to Limit the Rate of Incisional Hernia Occurrence"
protocolSection.statusModule.overallStatus
"ACTIVE_NOT_RECRUITING"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Incisional Hernia (protocolSection.conditionsModule.conditions)
  • Incisional Hernia of Midline of Abdomen (protocolSection.conditionsModule.conditions)
  • Midline Laparotomy (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.