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Female Pattern Hair Loss clinical trials

View clinical trials related to Female Pattern Hair Loss.

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NCT ID: NCT04090801 Completed - Clinical trials for Female Pattern Hair Loss

Comparison of Topical Minoxidil 5% in Ethanol Plus Propylene Glycol Versus Minoxidil 5% in Ethanol Alone in Treatment of Women With Female Pattern Hair Loss

FPHL
Start date: May 30, 2015
Phase: Phase 4
Study type: Interventional

The study will be included 60 women with FPHL. The diagnosis of FPHL will be established by clinical (Ludwig classification) and trichoscopic evaluation of frontal and occipital regions of the scalp.

NCT ID: NCT02206802 Completed - Alopecia Clinical Trials

Minoxidil Response Testing in Females With Female Pattern Hair Loss

Start date: July 2014
Phase:
Study type: Observational

The primary purpose of this study is to evaluate the clinical validity of the minoxidil response in-vitro diagnostic kit.

NCT ID: NCT01900041 Completed - Clinical trials for Female Pattern Hair Loss

A Study to Evaluate the Superiority, Efficacy and Tolerability of Combination Pantovigar With 2% Minoxidil vs 2% Minoxidil in Women With Female Pattern Hair Loss

Start date: April 2012
Phase: Phase 2
Study type: Interventional

Pantovigar - a high effective product designed primarily for the treatment of diffuse hair loss in women as well as for the treatment of damaged hair, in the combined therapy can be successfully applied in other types of alopecia. The purpose of this study is to evaluate efficacy and tolerability of combination therapy Pantovigar plus 2% minoxidil vs 2% minoxidil. To collect tolerability data for combined treatment Pantovigar plus 2% Minoxidil course therapy.

NCT ID: NCT00958750 Completed - Clinical trials for Androgenetic Alopecia

Efficacy and Safety Study to Compare Two Minoxidil Formulations on Women With Androgenetic Alopecia

Start date: June 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine in women the risk/benefit profile and non-inferiority of a topical 5% Minoxidil foam formulation applied once daily for the treatment of androgenetic alopecia in comparison to 2% MTS used twice daily, using objective and subjective efficacy measures and safety assessments for a study period of 24 weeks.

NCT ID: NCT00175617 Completed - Clinical trials for Female Pattern Hair Loss

Efficacy of Therapy With the Spironolactone Pills Compared to Minoxidil Lotion in Female Pattern Hair Loss

Start date: September 2005
Phase: Phase 2
Study type: Interventional

This study evaluates the efficacy of therapy with the anti-androgen spironolactone compared to topical minoxidil in female pattern hair loss.