Hyperhidrosis Clinical Trials

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Evaluation of the Efficacy of Botulinum Toxin Type A in the Treatment of Frontal Hyperhidrosis

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Frontal hyperhidrosis is a form of primary focal hyperhidrosis that significantly impairs patients' quality of life due to excessive visible sweating in the forehead region. Conventional treatment options often show limited efficacy or may be associated with undesirable side effects. This study aims to evaluate the efficacy and safety of intradermal injections of Botulinum Toxin Type A in patients with primary frontal hyperhidrosis. Clinical outcomes will be assessed using Minor's iodine-starch test, the Hyperhidrosis Disease Severity Scale (HDSS), and patient satisfaction scores. Participants will be followed up one month after treatment to evaluate therapeutic response and potential adverse effects.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 40
Healthy Volunteers: f
View:

• Patients aged between 18 and 40 years.

⁃ Clinically and objectively confirmed primary focal frontal hyperhidrosis, defined by sweat production \>50 mg/min and a Hyperhidrosis Disease Severity Scale (HDSS) score ≥3 (moderate to severe).

⁃ Inadequate response to topical antiperspirant therapy.

⁃ No prior treatment with Botulinum toxin type A within the last 6 months.

⁃ No use of any other hyperhidrosis treatment within the last 3 months.

Locations
Other Locations
Syrian Arab Republic
Latakia University Hospital
RECRUITING
Latakia
Contact Information
Primary
Zeinab Y Mohammad, MD
zeinab.y.mohammad@latakia-univ.edu.sy
+963937109668
Backup
Mohamad A Ismaiel, MD, PhD
mohamad.ismaiel@latakia-univ.edu.sy
‪+963933471500‬
Time Frame
Start Date: 2025-11-20
Estimated Completion Date: 2026-11-20
Participants
Target number of participants: 30
Treatments
Experimental: Botulinum Toxin Type A Group
Participants with primary frontal hyperhidrosis will receive intradermal injections of botulinum toxin type A in the affected frontal area. Injection sites will be identified using Minor's iodine-starch test, followed by standardized grid-based mapping to ensure precise localization and uniform distribution of the toxin across the hyperhidrotic region.
Related Therapeutic Areas
Sponsors
Leads: Tishreen University

This content was sourced from clinicaltrials.gov