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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03921320
Other study ID # Usaopaulo04032019
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 7, 2019
Est. completion date December 2023

Study information

Verified date October 2021
Source University of Sao Paulo
Contact Niura N Hamiltopn, MD
Phone +55 (11) 2661-5708
Email niurinhaa@yahoo.com.br
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The standard treatment for palmar hyperhidrosis is bilateral sequential thoracic sympathectomy. High rates of compensatory sweating due to the surgical procedure are described in the literature. In the search for a reduction in this side effect, it is possible that unilateral sympathectomy in the dominant side obtains acceptable results and leads to less compensatory sweating with improvement of the quality of life. The aim of this study it to compare the intensity of compensatory sweating due to the standard treatment, that is, bilateral sequential videothoracoscopic sympathectomy in relation to unilateral thoracic sympathectomy on the dominant side.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2023
Est. primary completion date June 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - Body mass index equal to or less than 28; - Exclusive palmar hyperhidrosis or palmar hyperhidrosis associated with axillary and / or plantar hyperhidrosis; Exclusion Criteria: - Being sinister (or left-handed); - Craneo-f acial or generalized hyperhidrosis; - Coagulopathies; - Previous thoracic surgery; - Other comorbidities such as cardiological, metabolic, infectious or neoplastic diseases; - Pregnancy;

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Bilateral sequential sympathectomy
Bilateral videothoracoscopic sequential R4 sympathectomy
Unilateral sympathectomy
Unilateral videothoracoscopic R4 sympathectomy in dominant side (right side)
Contralateral sympathectomy
Contralateral (left side) videothoracoscopic R4 sympathectomy

Locations

Country Name City State
Brazil Hospital Julia Kubitschek Belo Horizonte MG
Brazil Instituto Hospital de Base Brasília DF
Brazil Hospital Geral de Caxias do Sul Caxias do Sul RS
Brazil Hospital Geral Dr. Cesar Cals Fortaleza CE
Brazil Hospital Maternidade Terezinha de Jesus Juiz de Fora MG
Brazil Hospital Universitário da Universidade Federal do Amazonas Manaus AM
Brazil Hospital Universitário Onofre Lopes Natal RN
Brazil Hospital Universitário Oswaldo Cruz Recife PE
Brazil Hospital Universitário Pedro Ernesto Rio de Janeiro RJ
Brazil Hospital Santa Isabel Salvador BA

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Other Change of Quality of life To utilize the HidroQOL questionnaire to evaluate the change in quality of life Change from baseline quality of life to 6 months after surgery
Primary Change of sweating intensity To utilize the HDSS questionnaire to assessment of sweating intensity change in patients with palmar hyperhidrosis treated by bilateral sequential thoracic sympathectomy Change from baseline sweating to 6 months after surgery
Secondary Change of sweating intensity To utilize the HDSS questionnaire to assessment of sweating intensity change in patients with palmar hyperhidrosis submitted to unilateral sympathectomy on the dominant (right) side Change from baseline sweating to 6 months after sympathectomy
Secondary Change of sweating intensity To utilize the HDSS questionnaire to assessment of sweating intensity change in patients submitted to contralateral (left side) sympathectomy after unilateral sympathectomy on the dominant side Change from baseline sweating to 6 months after surgery