NCT05827913

Brief Summary

  1. 1.Striae distensae (SD), also known as stretch marks, are common, permanent dermal lesions that can be symptomatic and are considered aesthetically undesirable; thus, they pose a significant psychosocial and therapeutic challenge. SD arise in areas of dermal stretching and most commonly occur on the abdomen, breasts, buttocks, and thighs. Most literature has described SD during pregnancy(striae gravidarum) and puberty, with reported prevalences varying from 11% to 88%. Hormonal influences, reduced genetic expression of fibronectin, collagen, and elastin, and mechanical stretching of the skin have all been postulated to contribute to SD formation. In the acute phase, SD appear as red/violaceous lesions (striae rubrae; SR) that can be raised and symptomatic. The chronic form (striae albae; SA) exists as hypopigmented dermal depressions.
  2. 2.Polylevolactic Acid(PLLA) is at present one of the most promising biodegradable polymers (biopolymers) and has been the subject of abundant literature over the last decade. PLLA can be processed with a large number of techniques and is commercially available (large-scale production) in a wide range of grades.
  3. 3.Previous studies have found that 1565-nm laser can promote the synthesis of types I, III, and VII collagen and elastin, as well as the remodeling of dermal collagen. According to previous studies, dermal collagen deposition and remodeling may be related to the mechanism by which 1565-nm laser improves SD.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2023

Completed
28 days until next milestone

First Submitted

Initial submission to the registry

March 29, 2023

Completed
27 days until next milestone

First Posted

Study publicly available on registry

April 25, 2023

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2024

Completed
Last Updated

April 25, 2023

Status Verified

March 1, 2023

Enrollment Period

1 year

First QC Date

March 29, 2023

Last Update Submit

April 24, 2023

Conditions

Keywords

Polylevolactic AcidStriae Distensae1565nm Non-ablative Fractional Lasertreatment

Outcome Measures

Primary Outcomes (1)

  • The treatment effect is judged by color, area, concavity and convexity, and skin elasticity

    * Color: Ranked in order as follows: Purple red pink skin color, no change 0 point, 1 point added for each shade subtracted; * Area: 0 point: no change, 1 point: slightly improved, 2 points: significantly improved, 3 points: basically invisible; * Bump sensation: 0 point: no change, 1 point: slightly improved, 2 points: significantly improved, 3 points: bump basically eliminated; * Skin elasticity: 0 point: no change, 1 point: slightly improved, 2 points: significantly improved, 3 points: very satisfied; The total score of 6-12 points is basically cured; A total score of 3-5 points is significant; Effective with a total score of 1-2; A total score ≤ 1 is invalid. Total effective rate of treatment=(basically cured+significantly effective+effective)/total number of cases × 100%. Higher scores mean a better outcome.

    4months

Study Arms (3)

Polylevolactic Acid Injection

EXPERIMENTAL

Polylevolactic Acid Injection in SD

Device: Polylevolactic Acid Injection

Fractional Laser

ACTIVE COMPARATOR

1565nm Non-ablative Fractional Laser treatment in SD

Device: 1565nm Non-ablative Fractional Laser

combination treatment

ACTIVE COMPARATOR

Polylevolactic Acid injection combined with 1565nm Non-ablative Fractional Laser treatment in SD

Device: Polylevolactic Acid Injection combined with 1565nm Non-ablative Fractional Laser

Interventions

The patient was placed in a flat recumbent position and subjected to topical anesthesia with lidocaine cream for those who were unable to tolerate pain. According to the location and degree of indentation of the atrophic stria, a conventional disinfection towel is placed and injected into the subcutaneous and deep dermis. Use left thumb and index finger to press or tighten the skin from both sides to the middle. Depending on the location of the SD, determine the injection direction. During linear injection, the injection starts from the distal end of the SD, and then the injection is withdrawn until the SD subsides. Apply uniform force and withdraw the needle at a uniform speed. Stop the injection before the needle is pulled out of the skin, To avoid too shallow an injection.

Polylevolactic Acid Injection

M22-ResurFx laser (Lumenis Medical Company, USA) was used for treatment, with a wavelength of 1565 nm, a selected energy of 45 mJ, and a lattice density of 200 dots/cm2. The end point reaction was erythema and wind masses at the treatment site.

Fractional Laser

combination of the two treatments described above

combination treatment

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age: 18-50 years old, regardless of gender;
  • The clinical diagnosis was atrophic stria;
  • Patients with normal blood routine, liver and kidney function, and preoperative infection;
  • Able to communicate well with researchers and comply with the overall test requirements;
  • Willing to take and retain photos before and after treatment;
  • Volunteer and sign an informed consent form.

You may not qualify if:

  • Scar constitution;
  • Acute or chronic skin infections (including bacteria, viruses, and fungi) exist near the treatment area;
  • Those who are allergic to any component of the product;
  • Those who have been injected with anticoagulant drugs;
  • Those who have used other drugs, other substances, and other implant agents;
  • Patients with severe primary and psychiatric disorders such as heart, brain, liver, kidney, hematopoietic system, endocrine system, etc;
  • History of peripheral vascular disease, long-term alcoholism, diabetes, immunosuppression, disorder, drug abuse, etc;
  • Pregnant and lactating women;
  • Those who are critically ill and difficult to accurately evaluate the effectiveness and safety of the product.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dermatology Derpartment of Xijing Hospital

Xi'an, Shaanxi, 710032, China

RECRUITING

Related Publications (1)

  • Qu H, Wang L, Xin W, Lu M, Jing H, Wang G, Gao L. Clinical Efficacy Comparisons Between Poly-L-Lactic Acid Injections and Non-Ablative 1565-nm Fractional Laser for Treatment of Striae Distensae-A Randomized Trial. J Cosmet Dermatol. 2025 Jul;24(7):e70338. doi: 10.1111/jocd.70338.

MeSH Terms

Conditions

Striae Distensae

Condition Hierarchy (Ancestors)

Skin ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Gang Wang, Prof

    Dermatology Department of Xijing Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 29, 2023

First Posted

April 25, 2023

Study Start

March 1, 2023

Primary Completion

March 1, 2024

Study Completion

March 1, 2024

Last Updated

April 25, 2023

Record last verified: 2023-03

Locations