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Active clinical trials for "Alopecia"

Results 281-290 of 449

Pain Outcomes Following Intralesional Corticosteroid Injections

KeloidAlopecia Areata13 more

Corticosteroid therapy, including intralesional and topical applications, has many indications within the fields of Dermatology, Plastic Surgery, and Orthopedics. However, these injections can be quite painful, which leads many patients to discontinue treatment. Often, the injection involves a mixture of local anesthetic and corticosteroids despite a lack of evidence that the use of lidocaine improves pain. Due to the acidic pH, the lidocaine component of the injection can actually cause a significant burning sensation during the procedure. Lidocaine does not have anti-inflammatory properties and does not treat the underlying pathology. By including another medication, lidocaine also adds cost and risk to the procedure. The purpose of this study is to see if removing lidocaine from intralesional injections decreases the pain of injection.

Completed4 enrollment criteria

Hair Transplantation in Cicatricial Alopecia

Hair TransplantationCicatricial Alopecia

follicular unit extraction as a method of hair transplantation in cicatricial alopecia

Completed10 enrollment criteria

Superficial Cryotherapy Versus Microneedling in Alopecia Areata

Alopecia Areata

This study is randomized comparative analytical prospective study that included patients with mild and moderate alopecia areata. Patients was divided into two groups Patients in the first group underwent Superficial cryotherapy using dimethyl ether and propane (DMEP) at -57C (Cryotherapy group). Patients in the second group underwent Microneedling (Microneedling group). A total of six sessions were done at 2 weeks interval. Patients were followed-up for next 3 months to evaluate the persistence of hair regrowth after therapy. Patients were assessed at baseline and during follow up using photography, Dermoscopy, SALT score and regrowth scale.

Completed9 enrollment criteria

Comparison of Topical Minoxidil 5% in Ethanol Plus Propylene Glycol Versus Minoxidil 5% in Ethanol...

Female Pattern Hair Loss

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.

Completed2 enrollment criteria

A Phase 3 Clinical Study Patients With Androgenetic Alopecia (AGA)

AGA

A Multicenter, Randomized, Double-Blind, and Placebo-Controlled Phase 3 Clinical Study ,the mean change from baseline in vertex target area hair count (TAHC) after treatment for 24 weeks.

Completed13 enrollment criteria

A Study to Evaluate and Compare Injections of Autologous Mixed Population of Dermal Cells Cells...

Androgenetic AlopeciaMale Pattern Baldness1 more

Evaluate the ability of injections of Ji Gami(TM) CN to induce hair growth in male and female subjects with hair loss.

Completed23 enrollment criteria

A Study to Evaluate and Compare Injections of Autologous Dermal and Epidermal Cells Into the Balding...

Androgenetic AlopeciaMale Pattern Baldness1 more

Evaluate the ability of injections of Ji Gami(TM) and Ji Gami(TM) DO to induce hair growth in male and female subjects with hair loss.

Completed14 enrollment criteria

Enhancing Hair Density With Platelet Rich Fibrin Matrix (PRFM)

Alopecia

Clinical alopecia occurs due to miniaturization of the hair shafts as well as loss of active production of hair shafts. PRFM has been shown to induce dermal angiogenesis, and anecdotal findings of improvement of hair appearance after PRFM injection in the scalp suggest that PRFM may play a role in the treatment of thinning hair. Patients will be treated on a monthly basis with intradermal injections of autologous PRFM for 3 months. Changes in hair density will be assessed by comparing pre- and post-treatment photographs and non-invasive measurements of hair density at 1, 2, 3, 4 and 6 months after initial treatment.

Completed3 enrollment criteria

Optimizing Parameters for Long-pulsed Nd:YAG Laser for Reducing Hair Shaft Diameter

Androgenetic AlopeciaHair Loss/Baldness

This study evaluates the optimizing parameters of long pulse Nd:YAG Laser for reducing the size of hair shaft diameter of the donor for hair transplantation. All participants will receive long-pulsed Nd-YAG laser treatments with three different parameters at the occipital area.

Completed9 enrollment criteria

A Randomised Control Trial of Integrative Cognitive Behavioural Therapy for Alopecia

Alopecia

This Randomised Control Trial (RCT) aims to test a novel Alopecia-tailored, protocolled, integrative individual psychological intervention offered to patients with enduring Alopecia. The pilot study aims to assess the impact of the intervention on 8 patients, by assessing changes in their psychological and physical symptoms (stress, anxiety, depression, quality of life, scalp hair, and other bio-markers) compared to 7 patients in the wait-list control group.

Completed8 enrollment criteria
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