"Incidence of Compensatory Hyperhidrosis After T3 Vs T3-4 Sympathectomy"
"From One Problem to Another, Comparing the Incidence of Compensatory Hyperhidrosis After T3 Vs. T3-4 Sympathectomy"
1 other identifier
observational
46
0 countries
N/A
Brief Summary
The goal of this study is to compare the proportion of compensatory hyperhidrosis patients after sympathectomy at T3 level and sympathectomy at T3-4 level. The main question it aims to answer is: can sympathectomyv at one level decrease the incidence of compensatory hyperhidrosis after primary hyperhidrosis.
Trial Health
Trial Health Score
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participants targeted
Target at P25-P50 for all trials
Started Nov 2025
Typical duration for all trials
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 13, 2025
CompletedFirst Posted
Study publicly available on registry
September 29, 2025
CompletedStudy Start
First participant enrolled
November 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 20, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 25, 2028
October 3, 2025
September 1, 2025
1.9 years
September 13, 2025
September 30, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
To compare the incidence of compensatory hyperhidrosis following T3 versus T3-4 sympathectomy.
1 year post-sympathectomy
Secondary Outcomes (3)
severity of Compensatory hyperhidrosis by hyperhidrosis disease severity scale
1 year post sympathectomy
recurrence rates of primary hyperhidrosis
1 year post sympathectomy
site of compensatory hyperhidrosis
1year post sympathectomy
Study Arms (2)
T3 sympathectomy
patients who underwent T3 sympathectomy for primary hyperhidrosis
T3-4 sympathectomy
patients who underwent through T3-4 sympathectomy for primary hyperhidrosis
Eligibility Criteria
population of study are patients with primary hyperhidrosis who are going through T3 or T3-4 sympathectomy.
You may qualify if:
- Patients diagnosed with primary hyperhidrosis
- Patients with palmar and\\or axillary hyperhidrosis.
- Age ≥ 6 years
You may not qualify if:
- History of Prior thoracic surgery.
- History of prior disorder that cause hyperhidrosis ( obesity,autonomic neuropathy,menopause,gout,etc…)
- History of prior systemic diseases cause hyperhidrosis (hyperthyroidism,DM,pheochromocytoma,Parkinson's disease,etc…)
- Patients with psychological problems.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (7)
Faul F, Erdfelder E, Buchner A, Lang AG. Statistical power analyses using G*Power 3.1: tests for correlation and regression analyses. Behav Res Methods. 2009 Nov;41(4):1149-60. doi: 10.3758/BRM.41.4.1149.
PMID: 19897823BACKGROUNDStrutton DR, Kowalski JW, Glaser DA, Stang PE. US prevalence of hyperhidrosis and impact on individuals with axillary hyperhidrosis: results from a national survey. J Am Acad Dermatol. 2004 Aug;51(2):241-8. doi: 10.1016/j.jaad.2003.12.040.
PMID: 15280843BACKGROUND4. Lin TS, et al. Clinical experience of thoracoscopic sympathetic block for primary hyperhidrosis: analysis of 3450 cases. J Thorac Cardiovasc Surg. 2001;121(3):566-74.
BACKGROUND3. Hussein AF, et al. Unilevel (T3) versus Bilevel (T3 - T4) Sympathictomy in the Management of Palmar Hyperhidrosis: A Prospective Comparative Study. Clinics (Sao Paulo). 2024.
BACKGROUND2. Liu X, Wang J, Liu Z, Sun X, Zheng J. Comparison of only T3 and T3-T4 sympathectomy for axillary hyperhidrosis: a retrospective study. J Thorac Dis. 2018;10(4):2095-101.
BACKGROUNDFaul F, Erdfelder E, Lang AG, Buchner A. G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007 May;39(2):175-91. doi: 10.3758/bf03193146.
PMID: 17695343BACKGROUNDLicht PB, Pilegaard HK. Severity of compensatory sweating after thoracoscopic sympathectomy. Ann Thorac Surg. 2004 Aug;78(2):427-31. doi: 10.1016/j.athoracsur.2004.02.087.
PMID: 15276490BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 2 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal investigator
Study Record Dates
First Submitted
September 13, 2025
First Posted
September 29, 2025
Study Start
November 15, 2025
Primary Completion (Estimated)
October 20, 2027
Study Completion (Estimated)
October 25, 2028
Last Updated
October 3, 2025
Record last verified: 2025-09