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Lichen Sclerosus Et Atrophicus clinical trials

View clinical trials related to Lichen Sclerosus Et Atrophicus.

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NCT ID: NCT04107454 Active, not recruiting - Clinical trials for Lichen Sclerosus Et Atrophicus of the Vulva

Effect of Treatment With the Ablative Fractional Carbodioxide Laser in Vulvar Lichen Sclerosis

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Aim of this study is to evaluate the therapeutic effect of the laser treatment in vulvar LS, mainly the reduction of existing symptoms. As measured by visual analogue scale (VAS) symptoms as itching, burning, pain will be determined six weeks after the last laser treatment. Secondary endpoints will be sexual function measured with the female sexual function index (FSFI) and the vulvar skin changes measured by the Lichen score (LS). Regular photo-documentation of the treated skin will demonstrate a potential change of the tissue.

NCT ID: NCT04073082 Active, not recruiting - Clinical trials for Hidradenitis Suppurativa

Safety and Efficacy of Laser Therapy in Gynaecology

Start date: July 24, 2019
Phase:
Study type: Observational

The aim of this study is to retrospectively evaluate the effectiveness and safety of Er:YAG laser for treatment of different gynecological indication, e.g. genital lesions, Bartholin's cyst, condyloma, episiotomy scars, lesions of hydradenitis suppurativa and use of laser in genital surgery used in private practice.

NCT ID: NCT03926299 Active, not recruiting - Clinical trials for Vulvar Lichen Sclerosus

Clinical Trial to Demonstrate That the Dual Laser Therapy is Effective for the Treatment of Vulvar Lichen Sclerosus

Start date: July 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to test a new, minimally invasive dual laser technique to treat vulvar lichen sclerosus. Efficacy and safety of the thermal non-ablative Nd:YAG laser and the ablative Er:YAG laser is determined and compared to the current standard treatment with high dose steroids. The hypothesis is that laser therapy is effective and similar to standard steroid therapy.

NCT ID: NCT03525522 Active, not recruiting - Lichen Sclerosus Clinical Trials

Nd:Yttrium Aluminum Garnet Laser Treatment for Lichen Sclerosus

Start date: January 28, 2016
Phase: N/A
Study type: Interventional

This study evaluates the efficacy of Nd:Yttrium Aluminum Garnet Laser (Nd:YAG) Treatment of Lichen sclerosus in comparison with topical corticosteroid treatment. Half of participants will receive laser treatment and the other half corticosteroid treatment and the results will be followed for 6 months.