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Topical Oxybutynin for Treatment of Hyperidrosis: Local or Systemic Effect?

Launched by SAMANTHA RODRIGUES CAMARGO NEVES DE MOURA · Oct 27, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Hyperhidrosis Oxybutynin Anticholinergic Axillary Hyperhidrosis

ClinConnect Summary

The TODAY trial is studying a new treatment for excessive sweating, known as axillary hyperhidrosis, which affects the underarms. Researchers want to see if a special deodorant containing a medication called oxybutynin can help reduce sweating and if it has any side effects. This trial is currently looking for participants aged 18 to 45 who have not used any other treatments for their sweating for at least 30 days.

To join the study, you should not be allergic to oxybutynin, should not have any skin problems in your armpits, and if you're a woman who could become pregnant, you must be using birth control. Participants will apply the deodorant and be monitored for its effectiveness and safety. This is an exciting opportunity for those seeking relief from excessive sweating, and researchers are eager to see how well this new treatment works!

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients aged ≥18 years and ≤ 45 years
  • Not treated patient with another drug or treatment methodology for the disease for at least 30 days
  • Exclusion Criteria:
  • Patients who are hypersensitive to oxybutynin hydrochloride.
  • Not treated patient with another drug or treatment methodology for the disease for at least 30 days
  • Patients who have menopausal symptoms
  • Patients who show signs of skin lesions in the armpit
  • Pregnancy. Women with the potential to bear children should be under contraceptive strategies and take a negative pregnancy test to be enrolled
  • Patients with COVID in the contagious phase (PCR+)

About Samantha Rodrigues Camargo Neves De Moura

Samantha Rodrigues Camargo Neves de Moura is a dedicated clinical trial sponsor with a robust background in medical research and a commitment to advancing healthcare through innovative studies. With a focus on enhancing patient outcomes and ensuring ethical standards, she leads multidisciplinary teams in the design and execution of clinical trials across various therapeutic areas. Her expertise encompasses regulatory compliance, data management, and patient recruitment strategies, all aimed at fostering efficient trial processes and generating reliable results. Through her leadership, she strives to contribute to the scientific community and improve treatment options for patients globally.

Locations

São Paulo, Sp, Brazil

Patients applied

0 patients applied

Trial Officials

Eduardo Ramacciotti, MD, PhD

Study Chair

Science Valley Research Institute

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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