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

Retrospective Evaluation of Long Term Use of Oxybutynin in the Pharmacological Treatment of Primary Hyperhidrosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01956591
Enrollment
1100
Registered
2013-10-08
Start date
2007-09-30
Completion date
2013-09-30
Last updated
2013-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperhidrosis

Keywords

Treatment efficacy, Long-term effects, Tachyphylaxis, Undesirable effects, Side effects, Self-assessment, Hyperhidrosis, Quality of life

Brief summary

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

Detailed description

This retrospective study aims to evaluate the medical charts of patients who were treated with oxybutynin for at least six months for primary hyperhidrosis. The investigators variables of interest are: (1) quality of life before pharmacological therapy and after six weeks, (2)self-perception of improvement in hyperhidrosis after six weeks of treatment and on last visit (whenever this occur, as long as this happens after six months), (3) side effects related to drug use.

Interventions

DRUGOxybutynin

All patients are treated with oxybutynin for hyperhidrosis. Usual maintenance dose is 10mg/day, but dose may vary according to weight, efficacy and side effects. Our standard protocol starts with 2.5mg/day in the first 7 days, progresses to 5mg/day for 14 days and then reaches the usual maintenance dose of 10mg/day afterwards.

Sponsors

Hospital Israelita Albert Einstein
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
5 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Primary hyperhidrosis * At least 180 days of treatment with oxybutynin

Exclusion criteria

* Incomplete medical chart * Patients with glaucoma

Design outcomes

Primary

MeasureTime frameDescription
Quality of life1 day before treatmentEvaluate the Quality of life (using a standardized questionnaire for hyperhidrotic patients) before pharmacological treatment

Secondary

MeasureTime frameDescription
Perception of improvement in excessive sweatingAfter 42 days of treatmentWe want to analyze the patient's self perception (grades 0 to 10) of amelioration in sweating after forty-two days of treatment

Other

MeasureTime frameDescription
Side effects in the use of oxybutynin for hyperhidrosisAfter 42 days of treatmentAssess the side effects that have been reported on patient's charts, such as: dry mouth, constipation, headache, glaucoma, bowel obstruction and any other side effect reported

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026