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Axillary Hyperhidrosis clinical trials

View clinical trials related to Axillary Hyperhidrosis.

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NCT ID: NCT04546438 Completed - Clinical trials for Axillary Hyperhidrosis

Patient Satisfaction and Safety of Miradry Treatment for Axillary Hyperhidrosis

Start date: September 4, 2020
Phase: N/A
Study type: Interventional

Primary localized hyperhidrosis is a dermatological disorder that involves excessive sweat production without an underlying cause. The disease usually affects the axillae but can also involve palms, soles of the feet or face and causes major problems in many social situations with a negative impact on quality of life and mental health. In this study, the investigators want to investigate the effect of microwave therapy (MiraDry®) on self-rated sweating, quality of life and anxiety in participants with severe axillary hyperhidrosis. The study also aims to evaluate the safety (side effects) of the method and long term effects over 1 year of follow upp.

NCT ID: NCT03948646 Completed - Clinical trials for Axillary Hyperhidrosis

Safety and Efficacy Study of Sofpironium Bromide in Subjects With Axillary Hyperhidrosis (BBI-4000-CL-302)

CARDIGANII
Start date: December 4, 2020
Phase: Phase 3
Study type: Interventional

Hyperhidrosis is a disorder of abnormal excessive sweating. Primary hyperhidrosis (armpits, hands, and feet) affects approximately 4.8% of the US population and is believed to be caused by an overactive cholinergic response of the sweat glands. Current therapies have limited effectiveness, significant side effects, and can be invasive and costly. Sofpironium bromide (BBI-4000) is a novel soft-drug in development for the topical treatment of hyperhidrosis. This Phase 3 study will assess the safety and efficacy of sofpironium bromide, 15% gel versus vehicle (2 treatment arms), applied for the treatment of axillary hyperhidrosis.

NCT ID: NCT03836287 Completed - Clinical trials for Axillary Hyperhidrosis

Safety and Efficacy Study of Sofpironium Bromide in Subjects With Axillary Hyperhidrosis (BBI-4000-CL-301)

CardiganI
Start date: October 9, 2020
Phase: Phase 3
Study type: Interventional

Hyperhidrosis is a disorder of abnormal excessive sweating. Primary hyperhidrosis (armpits, hands, and feet) affects approximately 4.8% of the US population and is believed to be caused by an overactive cholinergic response of the sweat glands. Current therapies have limited effectiveness, significant side effects, and can be invasive and costly. Sofpironium bromide (BBI-4000) is a novel soft-drug in development for the topical treatment of hyperhidrosis. This Phase 3 study will assess the safety and efficacy of sofpironium bromide, 15% gel versus vehicle (2 treatment arms), applied for the treatment of axillary hyperhidrosis.

NCT ID: NCT03320096 Completed - Clinical trials for Axillary Hyperhidrosis

Evaluation of the Ulthera System for Treating Axillary Hyperhidrosis

ULT-218
Start date: December 13, 2016
Phase: N/A
Study type: Interventional

To evaluate the Ulthera System and the 7-3.0mm transducer for treating axillary hyperhidrosis.

NCT ID: NCT01274611 Completed - Clinical trials for Axillary Hyperhidrosis

Botox and Suction-Curettage for Treatment of Excessive Underarm Sweating (Axillary Hyperhidrosis)

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

The purpose of this study is to compare the effectiveness of two methods in the treatment of excessive underarm sweating (axillary hyperhidrosis): suction-curettage and Botox injections. Suction-curettage is a method in which the doctor will insert a suction tool into two small incisions in order to suction out the sweat-producing glands. It is similar to liposuction, but instead of suctioning out fat, the doctor suctions out the layer of the deep skin where the sweat glands are located. This method has been shown in some studies to effectively reduce underarm sweating for months at a time. Botox is a Food and Drug Administration (FDA) approved drug that in small doses, paralyses muscles. It is most commonly and famously used in the treatment of facial wrinkles. However, it has also been approved to treat excessive sweating. When injected in areas that sweat excessively, sweating can be significantly reduced in that area for months at a time. This study is a pilot study designed to determine feasibility of these procedures.

NCT ID: NCT01118429 Completed - Clinical trials for Axillary Hyperhidrosis

Use of Oxybutynin to Treat Axillary Hyperhidrosis

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

The objective of this study was to evaluate the effectiveness and patient satisfaction with the use of oxybutynin at low doses for treating axillary hyperhidrosis in a large series of patients.

NCT ID: NCT01091129 Completed - Clinical trials for Axillary Hyperhidrosis

Clinical Evaluation of the miraDry System in Subjects With Hyperhidrosis

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

The purpose of this study is to determine whether treatment by the miraDry System can safely reduce the severity of axillary hyperhidrosis (excessive underarm sweating).

NCT ID: NCT00735293 Completed - Clinical trials for Axillary Hyperhidrosis

VASER Treatment of Axillary Hyperhidrosis/Bromidrosis

VASER AxHH
Start date: April 2007
Phase: Phase 4
Study type: Interventional

Patients with excessive underarm odor and sweating and/or odor are treated with the VASER system to determine the VASER's effectiveness in reducing underarm sweat and odor