Treatment of Atrophic Post Acne Scars by Fat Grafting

Sponsor
Damascus University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05028283
Collaborator
(none)
69
1
1
27.4
2.5

Study Details

Study Description

Brief Summary

This single-center, clinical trial consists of a one autologous fat grafting treatment followed by1-week , 1month , 3-month and 6-month post-treatment visits in order to assess the efficacy and complications of fat grafting when used for facial atrophic acne scars on cheeks.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Fat Grafting
N/A

Detailed Description

This investigation, pilot study will evaluate the safety and efficacy of autologous fat grafting for the treatment of atrophic acne scarring on cheeks. Overall assessment of clinical outcome and safety will be based clinic visits and evaluation of pre- and post- procedural on the Goodman-Barron scale.

The subject's assessment of satisfaction will be characterized using a non-parametric assessment scale at the end of the follow-up period.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
69 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Autologous Fat Cells Transfer for the Treatment of Atrophic Post Acne Scars: Clinical Trail
Actual Study Start Date :
Aug 19, 2021
Anticipated Primary Completion Date :
Aug 19, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: participants

patients with atrophic acne scars on the cheeks who will reviewing the dermatological clinics at the Dermatology and Venereology Hospital at least 69 patients they will be undergo fat grafting for one session and will be follow up for 6 months after the procedure

Procedure: Fat Grafting
This single-center, clinical trial will assess the efficacy and tolerability of the autologous fat grafting when used on men and women with atrophic acne scars on the cheeks

Outcome Measures

Primary Outcome Measures

  1. • Change in atrophic acne scars assessment [Baseline and 6 Months]

    Acne scars will be used to evaluate efficacy of treatment using the Goodman- Barron scale [which is an acne scars severity scale divided into 4 grades First grade consists of hyper-or hypopigmented flat marks Second grade consists of mild atrophy or hypertrophy that may not be obvious at social distances of 50 cm or greater and may be covered adequately by makeup Third grade consists of moderate atrophic or hypertrophic scarring that is obvious at social distances of 50 cm or greater and is not covered easily by makeup or the normal shadow Fourth grade severe atrophic or hypertrophic scarring that is obvious at social distances of 50 cm or greater and is not covered easily by makeup or the normal shadow]. The grade of acne scars from final visit will be compared to their baseline grade visually evaluated by the study team.

  2. Change in patient satisfaction [3 Months, and 6 Months]

    The modified global aesthetic improvement scale for patient evaluation module which consists of 5 degrees Exceptionally improved [The ideal result has been achieve] much improved[The result is much improved but suboptimal] Improved[The result is improved but an additional procedure is recommended ] no difference[The result is the same when compared with the preoperative state] Worse[The result is worse when compared with the preoperative state] This module will be administered 3monts and 6 months postoperatively to analyze satisfaction and aesthetic perception of the result.

Secondary Outcome Measures

  1. Change in Infection existence [1 week, 1 month, 3 months and 6 Months]

    Patients will be examined after procedure to check existence of infection and will be monitored until it will heal.

  2. Change in Bruising Status [Baseline ,1 week 1 month,3 months and 6 Months]

    Patients will be examined after procedure to check bruising status and will be monitored until it will disappear

  3. Change in Erythema Presence [Baseline ,1 week ,1 month,3 months and 6 Months]

    Patients will be examined after procedure to check erythema presence and will be monitored until it will disappear

  4. Change in Swelling Status [Baseline ,1 week 1month,3 months and 6 Months]

    Patients will be examined after procedure to check swelling status and will be monitored until it will disappear

  5. Change in Irregularity Presence [Baseline and 6 Months]

    Patients will be examined after procedure to check irregularity presence at the end of the study

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with atrophic post acne scars on the cheeks, between 20 - 40 years old

  • Not to apply other treatments a month before the procedure

  • Informed consent to enter the study

Exclusion Criteria:
  • First grade of Goodman - Barron scale.

  • A systemic or associated skin disease that may affect the results of the study

  • patients with chronic consumption of nonsteroidal anti-inflammatory drugs (NSAIDs) or other non-aggregating agents.

  • Patients with acne in the acute stage

  • Pregnancy and breastfeeding

  • Tendency to form keloids

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dermatology and Venereology Hospital Damascus Syrian Arab Republic

Sponsors and Collaborators

  • Damascus University

Investigators

  • Principal Investigator: Rahaf Alkhouli, MSc, Dermatology Department, University of Damascus Medical School

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Damascus University
ClinicalTrials.gov Identifier:
NCT05028283
Other Study ID Numbers:
  • UDMS-Derma-01-2021
First Posted:
Aug 31, 2021
Last Update Posted:
Oct 11, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Damascus University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 11, 2021