Autologous fat injection into the face-

Comparing the longevity of normal autologous fat with autologous fat plus PRP in the face area (randomized double-blind clinical trial)

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250803066736N1

Enrollment

Registered

2025-09-26

Start date

2025-08-23

Completion date

Unknown

Last updated

2025-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention 1: Control group: Given that the age variable is an important confounding factor, in this study we will have 2 control groups as follows: Control group with an age range of 30 to 45 years

Eligibility

Sex/Gender

All

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Having dark circles and wrinkles on the face Complete patient consent to participate in the project Age 30 years and above and less than 60 years

Exclusion criteria

Exclusion criteria: Active wound or infection at the treatment site Receiving chemotherapy within the last 5 years Pregnancy or breastfeeding

Design outcomes

Primary

Measure	Time frame
WSRS scale (Wrinkle Severity Rating Scale). Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).;FVLS Scale (Facial Volume Loss Score). Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).;Body mass index. Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).	—

Measure

Time frame

WSRS scale (Wrinkle Severity Rating Scale). Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).;FVLS Scale (Facial Volume Loss Score). Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).;Body mass index. Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).

—

Secondary

Measure	Time frame
Patient satisfaction. Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).;Physician satisfaction. Timepoint: Before treatment, 1, 3 and 6 months after treatment. Method of measurement: Questionnaire (SERVQUAL).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. AfsanehSadeghzadeh Bazargan

Iran University of Medical Sciences

sadeghzadeh.a@iums.ac.ir+98 21 8670 2504

Outcome results