Stem cell assisted centrifugal fat transfer

Phase 3

Recruiting

• Conditions: Facial aging; Skin Aging; Aging

• Registration Number: RPCEC00000362
• Lead Sponsor: Hermanos Ameijeiras Surgical Clinical Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-03-26
• Study Completion: 2022-12-01
• Results First Posted: 2023-03-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

1. Patients between the ages of 30 and 59, without distinction of sex.
2. Patients with signs of facial aging.
3. Willingness to participate in the study, with prior written informed consent.
4. Compensated chronic diseases, if you suffer from them.

Exclusion Criteria

1. History of psychiatric disorders or coagulopathies.
2. Patients whose expectations cannot be achieved with the procedure.
3. Pregnant or lactating women.
4. Tendency to keloid.
5. Skin or systemic infection.
6. Patients who are on anticoagulant, antifibrinolytic or non-steroidal anti-inflammatory drugs (NSAIDs) or steroids.
7. History of having made facial lipotransfer or injected other substances as fillers in the face.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluation of the final result: (Good, Fair, Bad). Measurement time: 12 months after the intervention.

Secondary Outcome Measures

Name	Time	Method
1. Clinical evolution of furrows and wrinkles (Clinical response to treatment interpreted by doctor and patient, using the Global Aesthetic Improvement Scale (GAIS)] (Exceptional improvement. Total disappearance of wrinkles, Much improved. Marked partial response. Decrease in the number of wrinkles between 50 and 99%, Improved. Slight partial response. Decrease in the number of wrinkles less than 50%, No response. Same as at the beginning of treatment, Progression. Increased number or size of wrinkles )). Measurement time: 12 months after the intervention.<br>2. Satisfaction status: (Satisfied, Not satisfied). Measurement time: 12 months after the intervention. <br>3. Complications (Yes, No). Measurement time: 24 and 72 hours, 1 week and, 3, 6 and 12 months after the intervention.<br>4. Type of complications (Describe complications that appear). Measurement time: 24 and 72 hours, 1 week and, 3, 6 and 12 months after the intervention.