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Hyperhidrosis clinical trials

View clinical trials related to Hyperhidrosis.

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NCT ID: NCT02099695 Withdrawn - Hyperhidrosis Clinical Trials

Evaluate the Efficacy of Oxybutynin Chloride in Patients With Primary Hyperhidrosis

Start date: December 2015
Phase: Phase 3
Study type: Interventional

Treatment of primary hyperhidrosis through a comparative study between oxybutynin hydrochloride and placebo. Hydrochloride may decrease the symptoms of hyperhidrosis improving the subject's quality of life.

NCT ID: NCT02058264 Completed - Hyperhidrosis Clinical Trials

A Safety, Tolerability and Preliminary Efficacy Study of BBI-4000 in Subjects With Axillary Hyperhidrosis

Start date: February 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety, tolerability, pharmacokinetics and treatment effect of BBI-4000 when topically applied to subjects with axillary hyperhidrosis.

NCT ID: NCT02043145 Completed - Muscle Spasticity Clinical Trials

Safety and Efficacy of BOTOX® (Botulinum Toxin Type A) in Korea

Start date: July 2008
Phase: N/A
Study type: Observational

This post marketing surveillance study in Korea will evaluate the safety and efficacy of BOTOX (botulinum toxin Type A) in patients who receive treatment according to standard of care for primary axillary hyperhidrosis, focal spasticity or moderate to severe glabellar lines in clinical practice.

NCT ID: NCT02016885 Completed - Hyperhidrosis Clinical Trials

A Dose-Ranging Study of the Effect of Glycopyrrolate in Subjects With Axillary Hyperhidrosis

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

The purpose of this study is to evaluate the safety and efficacy of glycopyrrolate compared to vehicle for the treatment of axillary hyperhidrosis.

NCT ID: NCT01956591 Completed - Hyperhidrosis Clinical Trials

Long Term Results of the Use of Oxybutynin for the Treatment of Hyperhidrosis

Start date: September 2007
Phase: N/A
Study type: Observational

Evaluate the long term efficacy and side effects of oxybutynin in the treatment of hyperhidrosis.

NCT ID: NCT01934153 Completed - Hyperhidrosis Clinical Trials

Characterization of Exposure From Topical Administration of [14C] Umeclidinium to Axilla or Palm of Healthy Male Subjects

Start date: September 2, 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to characterize the pharmacokinetics (PK), safety and tolerability of topically applied umeclidinium following single dose topical administration. The results from this study will be used to 1) improve our understanding of the risk of systemic accumulation upon chronic administration, 2) support dosing recommendations in a 2a/2b study for axillary administration and, potentially, a separate combined 2a/2b study for palmar administration, and 3) confirm whether the same formulation can be used for axillary and palmar application for the next studies.

NCT ID: NCT01930604 Recruiting - Hyperhidrosis Clinical Trials

Botulinum Toxin Treatment in Craniofacial, Inguinal, Palmar, Plantar and Truncal Hyperhidrosis

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

Hyperhidrosis is defined as excessive sweating and affects about 2.8 % of the population. It has been shown to have a deleterious effect on the quality of life measured using the Dermatology Life Quality Index (DLQI) which is one of the most widely used dermatology-specific quality of life instruments. This is comparable to the effect on quality of life in patients with severe psoriasis of the skin as well as to nodulocystic acne patients before treatment with oral isotretinoin. The clinical effect of Botulinum Toxin (Btx) A has been established in three randomized controlled trials (RCT) in axillary hyperhidrosis. One RCT has indicated a positive effect in palmar hyperhidrosis. Although there is increasing evidence that Btx A and B have a similar effect on hyperhidrosis of other parts of the body (ie hyperhidrosis of the face, trunk, groin and feet) which is reported in case-reports and open studies there is still a great need for more controlled studies. This is why we will carry out this randomized, double-blind, placebo-controlled study to investigate the clinical effect and safety of Btx A in palmar, plantar and inguinal (groins/buttocks) hyperhidrosis and the clinical effect and safety of Btx B in craniofacial and truncal hyperhidrosis, respectively. Besides using the DLQI instrument we will also study Btx A/B to elucidate the impact of this treatment on quality of life using a generic instrument, the effect on anxiety and depressive symptoms, sweating, and patients´global assessment of therapy.

NCT ID: NCT01855256 Completed - Hyperhidrosis Clinical Trials

Treatment of Hyperhidrosis With Oxybutynin

H²O
Start date: June 2013
Phase: Phase 3
Study type: Interventional

Evaluation of the effectiveness of oxybutynin in hyperhidrosis

NCT ID: NCT01811004 Completed - Hyperhidrosis Clinical Trials

Evaluation of 1440nm Laser vs. Botulinum Toxin or miraDry® Microwave For Treatment of Axillary Hyperhidrosis

Start date: September 2012
Phase: N/A
Study type: Interventional

The Purpose of the study is to evaluate the 1440nm Laser Assisted Selective Photothermolysis vs. Botulinum Toxin or miraDry® Microwave Thermolysis For Treatment of Axillary Hyperhidrosis.

NCT ID: NCT01810991 Completed - HYPERHIDROSIS Clinical Trials

Investigation of Hyperhidrosis Treatment Using the Nd: YAG 1440nm Wavelength Laser

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the Nd:YAG 1440 nm wavelength laser for the treatment of primary hyperhidrosis of the axilla.