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Study identifier: NCT07126912 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of Efficacy and Safety of Alcarisa (Hyaluronic Acid Produced by Espad Pharmed Co.) for Restoration of Mid-face Volume

Condition: Mid Face Volume Deficit  ·  Sponsor: Espad Pharmed

PhaseNA
Planned participants30
Who can joinAll sexes, 30 Years to 65 Years
Healthy volunteersNo

About this study

Mid-face volume loss is a factor affecting beauty that makes people feel uncomfortable about themselves. The purpose of this study is to evaluate the efficacy and safety of Hyaluronic Acid injection with the brand name Alcarisa®, manufactured by Espad Pharmed Co., for treatment of this condition. The intervention consisted of a single treatment session, injecting 2 to 4 cc of gel into the zygomaticomalar area, and, if deemed by the physician, into the anteromedial cheek and submalar areas on each side of the face. The patient underwent digital photography at the following time points: before injection, immediately after injection, and at 4, 12, and 24 weeks post-injection. The physician then used these photographs to evaluate the product's efficacy and safety based on predefined measurements. In addition, participant satisfaction was assessed at the same time intervals.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (2)

Center for Research and Training in Skin Disease and LeprocyTehran, Tehran Province, IranRecruiting
Orchid Pharmed, Medical DepartmentTehran, Tehran Province, IranRecruiting

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Source record: clinicaltrials.gov/study/NCT07126912