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Alopecia Areata clinical trials

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NCT ID: NCT01017510 Recruiting - Alopecia Areata Clinical Trials

Comparative Study Examining the Effectiveness in Use of a DERMOJET and a Normal Syringe Treatment for Patients With Hair Loss - Alopecia Areata

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

Conventional treatments include the use of steroids applied locally, or injection in to the legion, or oral therapy. Treatment is determined by the severity of the disease. Injection in to the legion can be done in two methods 1. Subcutaneous injection syringe Lower 2. Using syringe DERMOJET - a syringe without a needle. So far there are no publications in the medical literature of studies comparing efficacy, safety, convenience of use for doctor-patient, of both methods.

NCT ID: NCT01016964 Completed - Clinical trials for Androgenetic Alopecia

Treatment of Androgenetic Alopecia in Females, 12 Beam

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the efficacy of the HairMax LaserComb 2009 12 beam model for androgenetic alopecia in females when treatment is applied as directed.

NCT ID: NCT01008774 Completed - Neoplasms Clinical Trials

START: Swiss Taxotere Alopecia Prevention Trial

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

Primary objective: - Rate of complete chemotherapy induced alopecia (WHO grade III or IV, physician grading) Secondary objective: - Compliance to scalp cooling procedure - Received number of cycles of chemotherapy in each subgroup - Patient perception of scalp cooling procedure - Side effects of scalp cooling systems

NCT ID: NCT01004809 Completed - Alopecia Clinical Trials

AVODART® Alopecia Post-marketing Surveillance (PMS)

AVODART®PMS
Start date: April 29, 2010
Phase:
Study type: Observational

Post-marketing surveillance(PMS) to monitor the safety and effectiveness of dutasteride in Korean androgenetic alopecia patients

NCT ID: NCT00999869 Recruiting - Alopecia Areata Clinical Trials

The Comparison Study of Intralesional Botulinum Toxin A and Corticosteroid Injection for Alopecia Areata

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

Alopecia areata is one of the most common cause of non-scarring alopecia. The pathogenesis is still unclear, however, it is believed to be an autoimmune disease. This disease is not a life-threatening condition but it has a significant psychological impact to patient's quality of life. Many triggers have been proposed such as viral infection, stress and neurologic factors. There are many studies show the correlation between disease activities and neurotransmitters level. Substance P and calcitonin gene-related peptide play major role in early stage of disease. These substances cause imbalance of CD4/CD8 lymphocyte in pathologic site and loss of immune privilege of hair follicles. The conventional treatment of alopecia areata with intralesional corticosteroid injection might treat the end of pathogenesis process. There is no therapeutic intervention for the origin of disease. Fortunately, botulinum toxin A could be a novel treatment of alopecia areata. The botulinum toxin A demonstrates inhibition release of substance P in many publications. To sum up, the treatment of alopecia areata with intralesional corticosteroid injection still be a standard treatment, nevertheless, patients have to receive this treatment every month until regrowth of scalp hair. Corticosteroid injection have several side effects, for example, skin atrophy, pigmentary change and hypothalamic-pituitary-adrenal axis suppression. Moreover, injection pain is also affect to psychological aspect . This study purpose is to evaluate the efficacy of botulinum toxin A for alopecia areata and reduce corticosteroid side effects, as well as, others opportunity cost. There is no prospective, randomized-controlled trial of comparison study between botulinum toxin A injection and corticosteroid injection for alopecia areata, therefore, investigators conduct this study for the greatest benefit to alopecia areata patients and for the future research in disease etiology.

NCT ID: NCT00999557 Withdrawn - Breast Cancer Clinical Trials

Bimatoprost Ophthalmic Solution in Increasing Eyebrow and Eyelash Growth in Patients Who Have Undergone Chemotherapy for Breast Cancer and in Healthy Participants

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

RATIONALE: Bimatoprost ophthalmic solution may help increase eyebrow and eyelash growth in patients who have undergone chemotherapy. PURPOSE: This randomized clinical trial is studying how wells bimatoprost ophthalmic solution works in increasing eyebrow and eyelash growth in patients who have undergone chemotherapy for breast cancer and in healthy participants.

NCT ID: NCT00997815 Completed - Clinical trials for Recalcitrant Alopecia Universalis

The Randomized Double-blind Placebo-controlled Trial of Intralesional Botulinum Toxin A Injection for Recalcitrant Alopecia Totalis and Alopecia Universalis

Start date: December 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The main purpose of this study is to determine the efficacy of intralesional botulinum toxin type A injection for recalcitrant alopecia totalis and alopecia universalis. Treatments of recalcitrant alopecia totalis and universalis remains an challenge issue for medical practice.The application of diphenylcyclopropenone (DPCP) is still being an standard treatment for the condition, however, there are at least thirty percentage of patients recalcitrant to this treatment. The complete etiology of this disease has yet to be clear.Nevertheless,recent studies have demonstrated the hypothesis of neurotransmitter involvements. There is numerous evidence in support of an imbalance of transmitters, including substance P and Calcitonin gene-related peptide. Botulinum toxin A injection has been used to treat a neuralgiform headache and diffused alopecia areata. Both headache and hair loss have been made much in improvement. This data may support the neurotransmitter imbalance theory. The investigators have been informed about possible effects to the alopecia condition, therefore, this study is conducted to assess the efficacy of botulinum toxin A as the novel treatment for recalcitrant alopecia totalis and alopecia universalis.

NCT ID: NCT00981461 Completed - Clinical trials for Androgenetic Alopecia

Treatment of Androgenetic Alopecia in Females, 9 Beam

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

The purpose of this study is to evaluate the efficacy of the HairMax LaserComb 2009 9 beam model in promoting hair growth in females diagnosed with androgenetic alopecia when treatment is applied as directed.

NCT ID: NCT00965640 Completed - Clinical trials for Male Pattern Baldness

Treatment of Male Pattern Baldness With Botulinum Toxin

Start date: December 2002
Phase: Phase 2
Study type: Interventional

This proof of concept study seeks to demonstrate that Botulinum toxin injections are a safe and effective method for treating this form of hair loss.

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.