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Use of Oxybutynin to Treat Axillary Hyperhidrosis

G

Grupo de Cirurgia Vascular

Status

Completed

Conditions

Axillary Hyperhidrosis
Osmidrosis

Treatments

Drug: Oxybutynin
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01118429
0083/10

Details and patient eligibility

About

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.

Enrollment

100 patients

Sex

All

Ages

14 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients with axillary hyperhidrosis

Exclusion criteria

  • glaucoma and micturition disorders, pregnancy

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 2 patient groups, including a placebo group

Oxybutynin
Experimental group
Description:
Oxybutynin was prescribed for 12 weeks, in progressively increasing doses throughout treatment. At their first visit, the patients were given 2.5 mg of oxybutynin into be taken once a day in the evening, were instructed to increase the dose to 2.5 mg twice a day from the eighth to the 42nd day, and to contact the doctor if they experienced any side effect. After this period they were seen in a second visit, and the dose was increased to 5 mg twice a day from the 43rd to the end of the 84thday, to when a third visit was scheduled.
Treatment:
Drug: Oxybutynin
Placebo
Placebo Comparator group
Description:
Oxybutyinine was prescribed for 12 weeks, in progressively increasing doses throughout treatment. At their first visit, the patients were given 2.5 mg of oxybutyn into be taken once a day in the evening, were instructed to increase the dose to 2.5 mg twice a day from the eighth to the 42nd day, and to contact the doctor if they experienced any side effect. After this period they were seen in a second visit, and the dose was increased to 5 mg twice a day from the 43rd to the end of the 84thday, to when a third visit was scheduled.
Treatment:
Drug: Placebo

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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