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Scalp Psoriasis clinical trials

View clinical trials related to Scalp Psoriasis.

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NCT ID: NCT03122353 Completed - Scalp Psoriasis Clinical Trials

BE Study of Calcipotriene Hydrate and Betamethasone Dipropionate Topical Suspension in the Treatment of Scalp Psoriasis

Start date: April 11, 2017
Phase: Phase 1
Study type: Interventional

This study will be conducted to evaluate the therapeutic bioequivalence of a TEST formulation of calcipotriene hydrate and betamethasone dipropionate topical suspension 0.005%/0.064% to the RLD.

NCT ID: NCT02933866 Completed - Scalp Psoriasis Clinical Trials

Phase III Clinical Study in Patients With Mild to Severe Scalp Psoriasis

Start date: March 11, 2016
Phase: Phase 3
Study type: Interventional

A Randomized, Double-Blind, Vehicle-Controlled, Parallel-Design, Multiple-Site, Phase III Clinical Study to Evaluate the Efficacy and Safety of DSXS topical product in Patients with Mild to Severe Scalp Psoriasis

NCT ID: NCT02933502 Completed - Scalp Psoriasis Clinical Trials

Safety Study in Patients With Scalp Psoriasis Suppression Following Maximal Use Treatment With Topical Product

Start date: July 11, 2016
Phase: Phase 2
Study type: Interventional

An Open-Label, Safety Study to Assess the Potential for Adrenal Suppression Following Maximal Use DSXS topical product (Taro Pharmaceuticals U.S.A., Inc.) in Patients with Moderate to SevereScalp Psoriasis

NCT ID: NCT02932462 Completed - Scalp Psoriasis Clinical Trials

Study to Evaluate Efficacy and Safety of the Topical Product in Patients With Mild to Severe Scalp Psoriasis

Start date: March 2016
Phase: Phase 3
Study type: Interventional

A Randomized Double-Blind, Vehicle-Controlled, Parallel Design, Multiple-Site, Phase III Clinical Study

NCT ID: NCT02749656 Recruiting - Scalp Psoriasis Clinical Trials

Efficacy and Safety of 0.25% Desoximetasone Cream (Topoxy®) in the Treatment of Scalp Psoriasis

Start date: January 1, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate efficacy and safety of 0.25% Desoximetasone cream (Topoxy®) compare with 0.25% Desoximetasone cream (Topicorte®) in the treatment of scalp psoriasis.

NCT ID: NCT02078297 Completed - Scalp Psoriasis Clinical Trials

IL-17 Role in Variants of Psoriasis

Start date: February 2014
Phase: N/A
Study type: Observational

The goal of this project is to study some mechanisms involved in the dysregulation of the immune system observed in the skin of subjects with psoriasis. This will be done by analyzing specific immune cells as well as gene and protein expression in small skin samples (biopsies) from patients with psoriasis. These results will be compared to the skin of healthy subjects without psoriasis.

NCT ID: NCT01914627 Completed - Scalp Psoriasis Clinical Trials

Parallel Group Trial to Evaluate the Efficacy and Safety of Loion® Compared to 10% Salicylic Acid in Patients With Chronic Psoriasis Capitis

Start date: August 2013
Phase: Phase 2
Study type: Interventional

The study will be conducted to evaluate the efficacy and safety of a topical dimeticone formulation (Loion®) compared to 10% salicylic acid in octyl-dodecanol with 15% Macrogol-4-laurylether for the removal of scaling in patients with chronic psoriasis capitis (scalp psoriasis).

NCT ID: NCT01558310 Not yet recruiting - Plaque Psoriasis Clinical Trials

A Study to Evaluate the Effectiveness of STELARA ™ (USTEKINUMAB) in the Treatment of Scalp Psoriasis

Start date: August 2012
Phase: Phase 4
Study type: Interventional

This is a single site, randomized, placebo-controlled, cross-over trial of sub-cutaneous injections of placebo and Stelara™ (ustekinumab) in subjects with scalp psoriasis.The purpose of the study is to assess the effectiveness of Stelara™ (ustekinumab)in the treatment of scalp psoriasis by determining the proportion of subjects who clear or almost clear in scalp specific physician assessments. The study will include approximately 30 subjects.

NCT ID: NCT01195831 Completed - Scalp Psoriasis Clinical Trials

Efficacy and Safety of Xamiol® Gel Compared to Calcipotriol Scalp Solution in Patients With Scalp Psoriasis

Start date: September 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the clinical efficacy of once daily treatment for 4 weeks with Xamiol® gel (calcipotriol plus betamethasone) with twice daily treatment for 4 weeks with Calcipotriol Scalp Solution in patients with scalp psoriasis.

NCT ID: NCT01120223 Completed - Scalp Psoriasis Clinical Trials

Safety and Efficacy of LEO 80185 Gel in Adolescent Subjects (Aged 12 to 17) With Scalp Psoriasis

Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of the study is to evaluate the safety and efficacy of once daily use of LEO 80185 gel in adolescent subjects (aged 12 to 17) with scalp psoriasis. LEO 80185 gel has marketing approval in many countries under the brand names Xamiol® gel and Taclonex Scalp® Topical Suspension for the treatment of scalp psoriasis in adults. No studies have been performed in subjects younger than 18 years