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Clinical trial

A Randomized, Subject- and Evaluator-blinded, Controlled, Non-inferiority Multicenter, Parallel Group Comparison Study to Evaluate Effectiveness and Safety of Saypha® VOLUME Lidocaine for Midface Augmentation to Correct Volume Deficit

NCT05386030 is registered in ClinicalTrials.gov with Croma-Pharma GmbH as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Subject- and Evaluator-blinded, Controlled, Non-inferiority Multicenter, Parallel Group Comparison Study to Evaluate Effectiveness and Safety of Saypha® VOLUME Lidocaine for Midface Augmentation to Correct Volume Deficit
Lead sponsor
Croma-Pharma GmbH
Phase
Phase 3
Overall status
Completed
Start date
August 16, 2022
Completion date
December 11, 2024
Enrollment
562 (actual)
Sites
16

Conditions

As the registry lists them; a condition with its own page is linked.

moderate to severe midface volume deficit