CLINICAL_TRIALS ClinicalTrials.gov record update

Clinical Study to Evaluate the Safety of the Viscoelastic Substance PRO-149 When Used as a Device During Phacoemulsification and Intraocular Lens Implantation in Patients With Age-related Cataract, Compared to Healon® EndoCoat.

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT04702802
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-25T22:28:49.807424+00:00
Published At: 2025-12-16T00:00:00+00:00
Record Updated At: 2025-12-16
Results Posted At: 2025-12-16
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Age-related Cataract", "Phacoemulsification"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2025-12-16"
protocolSection.identificationModule.nctId: "NCT04702802"
protocolSection.identificationModule.officialTitle: "Clinical Study to Evaluate the Safety of the Viscoelastic Substance PRO-149 When Used as a Device During Phacoemulsification and Intraocular Lens Implantation in Patients With Age-related Cataract, Compared to Healon\u00ae EndoCoat."
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2025-12-16"

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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