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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04090801
Other study ID # 5/2015
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date May 30, 2015
Est. completion date January 23, 2017

Study information

Verified date September 2019
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Enrolled women will be randomly assigned into 3 treatment groups: group A will apply topical minoxidil 5% in 90% ethanol and 5% propylene glycol, group B will apply topical minoxidil 5% in pure ethanol alone and group C will apply pure ethanol (placebo) twice daily.

The treatment will be continued for six months with regular visits at 3 months intervals.

The medications will be provided in bottles which were identical in shape and color, and were coded by a third party.

Both patients and investigator will be blinded to the medication. Disclosure of the codes will be done, by a third party, at the end of the study.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date January 23, 2017
Est. primary completion date May 30, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria:

- FPHL

Exclusion Criteria:

- No

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Topical minoxidil 5% in 90% ethanol and 5% propylene glycol

Topical minoxidil 5% in pure ethanol alone
The treatment will be continued twice daily.for six months with regular visits at 3 months intervals.
Other:
Placebo (Ethanol)
The treatment will be continued twice daily.for six months with regular visits at 3 months intervals.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Outcome

Type Measure Description Time frame Safety issue
Primary Ludwig scale grading system The 3 grades will be defined. Grade 1, (Thinning of hair is seen mainly over the anterior part of the crown with minimal widening of the parting width). Grade 2, (Thinning of the crown becomes more evident because of an increase in the number of thin and short hairs). Grade 3, (The crown becomes almost total bald, but the frontal hair line is still maintained). 0-6 months
Primary Trichoscopic examination of the hairs at frontal and occipital regions of the scalp. It will be evaluated signs of hair changes such as hair diameter diversity. 0-6 months
See also
  Status Clinical Trial Phase
Completed NCT00175617 - Efficacy of Therapy With the Spironolactone Pills Compared to Minoxidil Lotion in Female Pattern Hair Loss Phase 2
Withdrawn NCT02486848 - Minoxidil Dose Response Study in Females Identified Through IVD Testing as Non-Responders to 5% Topical Minoxidil N/A
Completed NCT00958750 - Efficacy and Safety Study to Compare Two Minoxidil Formulations on Women With Androgenetic Alopecia Phase 3
Completed NCT02206802 - Minoxidil Response Testing in Females With Female Pattern Hair Loss
Completed NCT01900041 - 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 Phase 2