Trials / Completed
CompletedNCT01118429
Use of Oxybutynin to Treat Axillary Hyperhidrosis
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Grupo de Cirurgia Vascular · Academic / Other
- Sex
- All
- Age
- 14 Years – 55 Years
- Healthy volunteers
- Not accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oxybutynin | 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. |
| DRUG | Placebo | 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. |
Timeline
- Start date
- 2007-01-01
- Primary completion
- 2009-06-01
- Completion
- 2009-06-01
- First posted
- 2010-05-06
- Last updated
- 2010-05-06
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT01118429. Inclusion in this directory is not an endorsement.