CLINICAL_TRIALS ClinicalTrials.gov record update

Phase I Clinical Study, to Evaluate the Safety and Tolerability of the Preservative-free Ophthalmic Solution PRO-087 Versus Xyel Ofteno® and Systane Ultra®, on the Ocular Surface of Ophthalmologically and Clinically Healthy Subjects

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT03524157
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:37:13.714917+00:00
Published At: 2019-07-19T00:00:00+00:00
Record Updated At: 2019-07-19
Results Posted At: 2019-07-19
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Dry Eye Syndromes", "Lubricant Allergy", "Tear Disorder"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2019-07-19"
protocolSection.identificationModule.nctId: "NCT03524157"
protocolSection.identificationModule.officialTitle: "Phase I Clinical Study, to Evaluate the Safety and Tolerability of the Preservative-free Ophthalmic Solution PRO-087 Versus Xyel Ofteno\u00ae and Systane Ultra\u00ae, on the Ocular Surface of Ophthalmologically and Clinically Healthy Subjects"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2019-07-19"

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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