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Clinical Trial

Effectiveness and Safety of Cellbooster Shape in Healthy Subjects

NCT: NCT07636512 · RECRUITING

NCT IDNCT07636512
StatusRECRUITING
Start Date2026-03-31
Completion2026-08-25
SponsorSuisselle (INDUSTRY)
First posted
Last updated

Brief Summary

SUISSELLE has developed a CE marketed (2021) HA-based superficial epidermis/dermis injection filler and skinbooster product, Cellbooster® Shape (CBS). CBS is produced using patented CHAC Technology. It consists of non-crosslinked HA with L-Carnitine and vitamin C. The device is particularly designed for reducing local puffiness by improving microcirculation and hydration. The current post-market clinical investigation is designed to evaluate the efficacy and safety of CBS. For this purpose, healthy subjects with signs of skin aging in the face will receive a 3-session treatment and will be followed-up over 70 days after the initial injection session. Several objective measurements of skin quality will be performed with different instruments allowing to assess skin volume, skin elasticity, skin hydration, and skin microcirculation. Subjective clinical improvement will be evaluated, as well as subject and investigator satisfactions. The safety of the injections will be assessed by collecting the Injection Site Reactions (ISRs) and Adverse Events (AEs).

Frequently Asked Questions

What is Effectiveness and Safety of Cellbooster Shape in Healthy Subjects?

Effectiveness and Safety of Cellbooster Shape in Healthy Subjects is a clinical trial registered under NCT07636512. Current status: RECRUITING.

What is the status of NCT07636512?

The current status of NCT07636512 (Effectiveness and Safety of Cellbooster Shape in Healthy Subjects) is: RECRUITING.

When did Effectiveness and Safety of Cellbooster Shape in Healthy Subjects start?

Effectiveness and Safety of Cellbooster Shape in Healthy Subjects started on 2026-03-31.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.