Evaluate the Safety and Efficacy of AGE Serum in Post-menopausal Patients on Hormone Replacement Therapy Taking Glucagon-like Peptide-1 Agonist

ConditionLaxity; Skin
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age45-65
SponsorGoldman, Butterwick, Fitzpatrick and Groff

About this trial

The primary objective is to assess the safety and efficacy of the AGE Serum in improving the appearance of skin in post-menopausal subjects on HRT and non-HRT who are takingGLP-1 agonist therapy through the use of investigator assessments, subject questionnaires/assessments, photography, skin imaging, and reported adverse reactions.

Eligibility criteria

Qualifiers

Post-menopausal women (25 on HRT, 25 non HRT all must be post-menopausal)

Presence of mild to moderate signs of facial aging (e.g., fine lines, laxity, dull texture) based on modified Griffith scale.

Adult women aged 45-65 years.

Fitzpatrick skin types I-VI.

Disqualifiers

Non post-menopausal state.

Any uncontrolled systemic disease.

History of autoimmune connective tissue disease.

Current use of immunosuppressive medication.

Trial design

Treatments tested in this trial

  • On GLP1 plus HRT
  • On GLP1 Only

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators