The Efficacy in Treatment of Female Pattern Hair Loss Using 5% Minoxidil Solution Combinded With Zinc Supplement
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|ClinicalTrials.gov Identifier: NCT01662089|
Recruitment Status : Unknown
Verified August 2012 by Rattapon Thuangtong, Siriraj Hospital.
Recruitment status was: Recruiting
First Posted : August 10, 2012
Last Update Posted : August 10, 2012
|Condition or disease||Intervention/treatment||Phase|
|Female Pattern Alopecia||Drug: 15 mg Chelate zinc supplement Drug: Placebo drug supplement||Phase 1 Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||20 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Official Title:||A Pilot Study of the Efficacy in Treatment of Female Pattern Hair Loss Using 5% Minoxidil Solution Combinded With Oral Chelated Zinc Supplement|
|Study Start Date :||January 2012|
|Estimated Primary Completion Date :||October 2012|
|Estimated Study Completion Date :||December 2012|
Experimental: Chelate zinc suppliment
15mg Chelate zinc suppliment : additional to standard 5% minoxidil
Drug: 15 mg Chelate zinc supplement
15 mg Chelate zinc additional to standard 5% minoxidil
Other Name: zinc, Zn
Placebo Comparator: Placebo drug
Placebo drug to compare with 15mg chelated Zn : additional to standard 5% minoxidil
Drug: Placebo drug supplement
Placebo drug instead of Zinc supplement
Other Name: starch
- Compare clinical improvement before and after treatment [ Time Frame: 6 month ]Measure clinical by Global photographic view using 7 point scale. Review picture by 2 dermatologist
- Compare hair density before and after treatmen [ Time Frame: 6 month ]Measure Hair density by microscope photo of area 1 cm2. Conut number of hair in photo.
- Compare average hair shaft diameter before and after treatment [ Time Frame: 6 month ]Compare average hair shaft diameter before and after treatment Measure hair shaft diameter using electronic outside micrometer.
- Number of pateint with Side effect [ Time Frame: 6 month ]Using side effect record form to record side effect from treatment Count number of pateint with side effect.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01662089
|Contact: Rattapon Thuangtong, MD||+662 419-7000 ext firstname.lastname@example.org|
|Bangkok, Thailand, 10700|
|Contact: Rattapon Thuangtong, MD +662 419-7000 ext 4333 email@example.com|