CLINICAL_TRIALS ClinicalTrials.gov record update

A Prospective, Multi-Center, Randomized, Controlled, Subject- and Evaluator-Blinded, Non-Inferior Clinical Investigation of the Safety and Effectiveness of TEOSYAL® PureSense ULTRA DEEP Versus Restylane® Lidocaine for the Correction of Moderate to Severe Nasolabial Folds in Chinese Adults

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06367634
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:39:49.951925+00:00
Published At: 2024-04-16T00:00:00+00:00
Record Updated At: 2024-04-16
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: ["Nasolabial Folds"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2024-04-16"
protocolSection.identificationModule.nctId: "NCT06367634"
protocolSection.identificationModule.officialTitle: "A Prospective, Multi-Center, Randomized, Controlled, Subject- and Evaluator-Blinded, Non-Inferior Clinical Investigation of the Safety and Effectiveness of TEOSYAL\u00ae PureSense ULTRA DEEP Versus Restylane\u00ae Lidocaine for the Correction of Moderate to Severe Nasolabial Folds in Chinese Adults"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: ["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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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