Treatment of Atrofic Striae With Percutaneous Collagen Induction Therapy Versus Fractional Nonablative Laser

Sponsor
Hospital de Clinicas de Porto Alegre (Other)
Overall Status
Completed
CT.gov ID
NCT03390439
Collaborator
Associação Fundo de Incentivo à Pesquisa (Other), MTO Importadora e Distribuidora (Other), Vydence Medical (Other), Aché Laboratórios Farmacêuticos Ltda (Industry)
20
1
2
9.6
2.1

Study Details

Study Description

Brief Summary

As atrophic striae are common dermatological conditions. Various therapeutic modalities have been employed in the treatment of striae distensae, mainly in striae rubra. There are few studies that include the treatment of striae alba.

The non-ablative fractionated laser and, more recently, microneedling are two distinct treatments, but they are widely used in dermatologist practice.

The present randomized clinical trial is aimed at evaluating and evaluating the response of microneedle and fractional non-ablative laser Nd-yap 1340 in the treatment of abdominal striae alba.

Condition or Disease Intervention/Treatment Phase
  • Device: Nd-Yap 1340nm laser
  • Device: Microneedling
N/A

Detailed Description

Twenty patients will be treated at the dermatologic clinic of the Hospital de Clínicas de Porto Alegre (HCPA). Each patient will be treated with laser and microneedle at the same time, being applied a therapeutic procedure in each part of the abdomen (divided lengthwise and in equal parts). Each part of the abdomen will be randomized for the treatment of laser or microneedling with the help of the Excel 2013 program. The investigator responsible for procedures and patients are the only ones with unblinded assessment in relation to the side of each treatment. There will be 5 sessions with monthly intervals of the proposed treatments. The ND-yap 1340-nm laser will be used, and in the other segment of the abdomen, the dermaroller 2.5 mm was applied. Photographic records of patients will be performed at pre-treatment and 1 month after the third and fifth sessions. The questionnaires will be applied to assess the quality of life in dermatology DLQI (Dermatology Life Quality Index). Two independent and blind evaluators for the type of treatment will apply in the Global Aesthetic Scale (GAIS) in the evaluation of photographic records. Cutaneous biopsies for histopathological evaluation will be performed with a punch 3 mm of each part of the abdomen at pretreatment. Two experienced pathologists will evaluate the measurements of the epidermis and the collagen and elastic fibers of the skin.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Each patient will have the abdomen divided equally. Each segment of the abdomen will be randomized using the Excel 2013 program to receive laser or microneedle treatment.Each patient will have the abdomen divided equally. Each segment of the abdomen will be randomized using the Excel 2013 program to receive laser or microneedle treatment.
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
Clinical evaluators will evaluate the photos after the treatments blindly for which type of treatment applied. Evaluators of skin biopsies will be blinded to what type of treatment is applied and for pre-treatment and post-treatment.
Primary Purpose:
Treatment
Official Title:
Treatment of Atrofic Striae With Percutaneous Collagen Induction Therapy Versus Fractional Nonablative Laser: a Randomized Trial
Actual Study Start Date :
Jul 1, 2017
Actual Primary Completion Date :
Apr 10, 2018
Actual Study Completion Date :
Apr 20, 2018

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Nd-Yap 1340nm laser

The randomly assigned segment of the abdomen will receive 5 sessions with monthly intervals of Nd-yap 1340nm laser.

Device: Nd-Yap 1340nm laser
Each part of the abdomen will be treated with a therapeutic modality. The ND-yap 1340-nm laser will be used in the following parameters: 90 mtz / cm2 nozzle, 90 mJ / mtz power, 2.5 Hz frequency, 3 ms pulse duration, 1 pass.
Other Names:
  • Nonablative Fractional Laser
  • Experimental: Microneedling

    The randomly assigned segment of the abdomen will receive 5 sessions with monthly intervals of dermaroller 2,5mm.

    Device: Microneedling
    In the other segment of the abdomen, the dermaroller 2.5 mm will be applied, with ten to fifteen passes in the same direction and at least four crosses in the rolling areas.
    Other Names:
  • Dermaroller
  • Percutaneous Collagen Induction Therapy
  • Outcome Measures

    Primary Outcome Measures

    1. Clinical response in abdominal alba striae after the therapies [6 months]

      Clinical response to microneedle treatment and nonablative fractional laser treatment without abdominal alba striae (GAIS scale). The GAIS scale is a non-numerical scale divided into 5 categories of clinical response: very much improved, much improved, improved, no changed and worse.

    Secondary Outcome Measures

    1. Clinical response to microneedle treatment and nonablative fractional laser treatment [4 months]

      Clinical response to microneedle treatment and nonablative fractional laser treatment without abdominal alba striae (GAIS scale). The GAIS scale is a non-numerical scale divided into 5 categories of clinical response: very much improved, much improved, improved, not changed and worse.

    2. Histopatological response in abdominal striae alba after the therapies [4 months]

      Histopathological evaluation of the thickness of the epidermis, as collagen and elastic (picrosirius stain, orcein stain)

    3. Histopatological response in abdominal striae alba after the therapies [6 months]

      Histopathological evaluation of the thickness of the epidermis, as collagen and elastic (picrosirius stain, orcein stain)

    4. The tolerability and incidence of adverse effects during the therapies [1 month]

      To assess the tolerability and the incidence of immediate and late adverse effects (pain, skin erythema, pruritus) for both techniques

    5. The tolerability and incidence of adverse effects during the therapies [2 months]

      To assess the tolerability and the incidence of immediate and late adverse effects (pain, skin erythema, pruritus) for both techniques

    6. The tolerability and incidence of adverse effects during the therapies [3 months]

      To assess the tolerability and the incidence of immediate and late adverse effects (pain, skin erythema, pruritus) for both techniques

    7. The tolerability and incidence of adverse effects during the therapies [4 months]

      To assess the tolerability and the incidence of immediate and late adverse effects (pain, skin erythema, pruritus) for both techniques

    8. The tolerability and incidence of adverse effects during the therapies [5 months]

      To assess the tolerability and the incidence of immediate and late adverse effects (pain, skin erythema, pruritus) for both techniques

    9. The impact on the quality of life provided by the striae distensae [Pre-treatment (first day of the evaluation)]

      To evaluate the impact on the quality of life (DLQI) provided by the striae. It is a simple 10-question validated questionnaire that has been used in over 40 different skin conditions.The DLQI is the most frequently used instrument in studies of randomised controlled trials in dermatology. The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired. 0-1: no effect at all on patient's life 2-5: small effect on patient's life 6-10: moderate effect on patient's life 11-20: very large effect on patient's life 21-30:extremely large effect on patient's life

    10. The impact on the quality of life provided by the striae distensae [4 months]

      To evaluate the impact on the quality of life (DLQI) provided by the striae. It is a simple 10-question validated questionnaire that has been used in over 40 different skin conditions.The DLQI is the most frequently used instrument in studies of randomised controlled trials in dermatology. The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired. 0-1: no effect at all on patient's life 2-5: small effect on patient's life 6-10: moderate effect on patient's life 11-20: very large effect on patient's life 21-30:extremely large effect on patient's life.

    11. The impact on the quality of life provided by the striae distensae [6 months]

      To evaluate the impact on the quality of life (DLQI) provided by the striae. It is a simple 10-question validated questionnaire that has been used in over 40 different skin conditions.The DLQI is the most frequently used instrument in studies of randomised controlled trials in dermatology. The DLQI is calculated by summing the score of each question resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired. 0-1: no effect at all on patient's life 2-5: small effect on patient's life 6-10: moderate effect on patient's life 11-20: very large effect on patient's life 21-30:extremely large effect on patient's life.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • female patients,

    • age 18 and over;

    • presenting with abdominal striae rubra diagnosed after clinical examination;

    • patients with weight stability in the last four months;

    • patients with Fitzpatrick III or IV phototype.

    Exclusion Criteria:
    • pregnant women;

    • childbirth for less than 12 months;

    • history of keloid scars;

    • presence of localized or systemic infection;

    • presence of immunosuppression;

    • use of photosensitizing medications;

    • use of systemic steroids;

    • use of oral isotretinoin in the last 12 months;

    • history of diseases of collagen or elastic fibers;

    • hypersensitivity to infiltrative or topical anesthetics;

    • patients who have been treated for striae distensae in the last year;

    • presence of sun exposure during the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ana Paula Naspolini Porto Alegre Rio Grande Do Sul Brazil 90035903

    Sponsors and Collaborators

    • Hospital de Clinicas de Porto Alegre
    • Associação Fundo de Incentivo à Pesquisa
    • MTO Importadora e Distribuidora
    • Vydence Medical
    • Aché Laboratórios Farmacêuticos Ltda

    Investigators

    • Study Director: Tania F Cestari, Dr, Hospital de Clínicas de Porto Alegre

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Hospital de Clinicas de Porto Alegre
    ClinicalTrials.gov Identifier:
    NCT03390439
    Other Study ID Numbers:
    • 47639415.1.0000.5327
    First Posted:
    Jan 4, 2018
    Last Update Posted:
    Aug 1, 2018
    Last Verified:
    Jun 1, 2017
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Hospital de Clinicas de Porto Alegre
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 1, 2018