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Alopecia clinical trials

View clinical trials related to Alopecia.

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NCT ID: NCT00926211 Completed - Clinical trials for Androgenetic Alopecia

Computer-Assisted Versus Manual Hair Harvest Comparative Study

Start date: June 2009
Phase: N/A
Study type: Interventional

The objective of this clinical study is to investigate and compare the safety and efficacy of the Restoration Robotics Computer-Assisted Harvesting System to the manual hair follicle harvesting method following a nine-month period of post-procedural evaluation.

NCT ID: NCT00691769 Completed - Clinical trials for Discoid Lupus Erythematosus

Expression of Fas Protein in Skin Biopsies of Participants With Scarring Alopecia

Start date: April 26, 2006
Phase:
Study type: Observational

The purpose of this research study is to see if a specific protein that we are interested in is involved in scarring hair loss. If these proteins are involved, further genetic work may also better define the disease as well as future treatment options.

NCT ID: NCT00515762 Completed - Breast Cancer Clinical Trials

Prevention of Persistent Alopecia Following Docetaxel by Means of Scalp Cooling

Start date: May 2007
Phase: Phase 2
Study type: Interventional

Persistent alopecia following adjuvant docetaxel for breast cancer is a side-effect that has been recently described. This pilot trial explores the capacity of a cooling cap (Elasto-gel) to prevent persistent alopecia in breast cancer patients treated with adjuvant docetaxel regimens.

NCT ID: NCT00484679 Completed - Alopecia Areata Clinical Trials

Adrenal Function and Use of Intralesional Triamcinolone Acetonide 10 mg/mL (Kenalog-10) in Patients With Alopecia Areata

Start date: May 2007
Phase: Phase 2
Study type: Interventional

The purpose of the study is to see whether treating alopecia areata with injections of the corticosteroid, Triamcinolone acetonide 10mg/cc (Kenalog-10), has an impact on the adrenal glands.

NCT ID: NCT00441116 Completed - Alopecia Clinical Trials

A Study To Assess The Efficacy And Safety Of Dutasteride 0.5mg Once Daily For 6 Months In The Treatment Of Male Subjects With Androgenetic Alopecia

Start date: December 15, 2006
Phase: Phase 3
Study type: Interventional

The aim of this Phase III study is to compare the efficacy, safety and tolerability of dutasteride (0.5mg) with placebo for 6 months, in Korean male subjects with androgenetic alopecia in the vertex region, types IIIv, IV and V according to the modified Norwood-Hamilton Classification.

NCT ID: NCT00418730 Completed - Clinical trials for Androgenetic Alopecia

Efficacy Study of Topical NEOSH101 to Treat Male Pattern Hair Loss

Start date: January 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to measure the hair growth response to topical NEOSH101 when applied twice daily to the balding scalp for 16 weeks. One hundred eighty men with Norwood/Hamilton grades III-IV with thinning in the top and center of the scalp will participate. Three equally sized treatment groups (60 men each) will receive either topical NEOSH101 2.0%, minoxidil 5%, or placebo.

NCT ID: NCT00408798 Completed - Alopecia Areata Clinical Trials

Treatment of Alopecia Areata of the Scalp With Intradermal Injections of Botulinum Toxin

Start date: October 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to examine prospectively the safety and efficacy of Botulinum Toxin A (Botox) injections in the treatment of patients with alopecia areata of the scalp.

NCT ID: NCT00396175 Completed - Clinical trials for Androgenetic Alopecia

Effects of Finasteride on Serum Prostate-Specific Antigen (0906-111)

Start date: March 1998
Phase: Phase 3
Study type: Interventional

A clinical study to collect additional data in order to characterize the reduction in PSA with finasteride 1 mg, and its reversibility in men with androgenetic alopecia between the ages of 40 to 60 years.

NCT ID: NCT00187577 Completed - Alopecia Areata Clinical Trials

Efficacy Study of Latanoprost and Bimatoprost Solutions in Promoting Eyelash Growth in Patients With Alopecia Areata

Start date: June 2005
Phase: N/A
Study type: Interventional

This is a single center, randomized, investigator-masked study to determine the efficacy and safety of latanoprost and bimatoprost ophthalmic solutions in promoting eyelash growth in patients who have lost their eyelashes due to alopecia areata. These medications are FDA-approved as eyedrops for patients with glaucoma who have been noted to grow longer, darker, and thicker eyelashes with their use. In this study, patients will be asked to apply these solutions to the affected eyelid margins of one eye with a sterile cotton-tipped applicator once a day.

NCT ID: NCT00179348 Completed - Depression Clinical Trials

Yoga-Based Rehabilitation Program in Reducing Physical and Emotional Side Effects in Patients With Cancer

Start date: February 8, 2001
Phase: N/A
Study type: Interventional

This clinical trial studies yoga-based rehabilitation in reducing physical and emotional side effects of living with cancer or its treatment. Yoga-based rehabilitation may reduce side effects and improve the quality of life of patients with breast, lung, or colorectal cancer.