Status:
COMPLETED
Skin Conduction Device and Patient Diary for Measuring Hot Flashes in Postmenopausal Women With Hot Flashes
Lead Sponsor:
Mayo Clinic
Collaborating Sponsors:
National Cancer Institute (NCI)
Conditions:
Hot Flashes
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
RATIONALE: Measuring how often hot flashes occur in postmenopausal women may be done by using a skin conduction device or by using a diary. PURPOSE: This clinical trial is studying a skin conduction ...
Detailed Description
OBJECTIVES: * Determine the differences in frequency, severity, and duration of hot flash activity using an ambulatory sternal skin conductance recording tool and patient hot flash diary in postmenop...
Eligibility Criteria
Inclusion
- DISEASE CHARACTERISTICS:
- Diagnosis of bothersome hot flashes, defined by their occurrence ≥ 4 times/day
- Daily hot flashes that have been present for ≥ 1 month
- PATIENT CHARACTERISTICS:
- Female
- Postmenopausal
- ECOG performance status 0-1
- No history of allergic or other adverse reactions to adhesives
- No other medical condition known to cause sweating and/or flushing
- No implanted pacemakers or metal implants
- No reliance on electronic devices for regular monitoring (i.e., insulin pumps or blood pressure monitors)
- PRIOR CONCURRENT THERAPY:
- Not specified
Exclusion
Key Trial Info
Start Date :
June 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 1 2006
Estimated Enrollment :
3 Patients enrolled
Trial Details
Trial ID
NCT00427531
Start Date
June 1 2006
End Date
September 1 2006
Last Update
March 17 2011
Active Locations (1)
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1
Mayo Clinic
Rochester, Minnesota, United States, 55905