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Clinical Trial Summary

The objectives of this study are to evaluate the effectiveness of an antiperspirant in preventing or attenuating the severity of palmer-plantar erythrodysesthesia associated with the Food and Drug Administration (FDA)-approved doses of capecitabine. The hypothesis is that cytotoxic compounds in sweat will be prevented from being deposited in the skin and causing chronic toxicity.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00213993
Study type Interventional
Source University of Wisconsin, Madison
Contact
Status Completed
Phase Phase 2
Start date May 2005
Completion date January 2007

See also
  Status Clinical Trial Phase
Completed NCT00992706 - F511 Cream in Preventing Palmar-Plantar Erythrodysesthesia in Patients Receiving Doxorubicin Hydrochloride Liposome for Metastatic Breast Cancer Phase 3
Recruiting NCT05939726 - Efficacy and Safety of Moisturising Cream With or Without Vitamin E and Urea Cream in Palmar-plantar Erythrodysesthesia N/A
Terminated NCT00486213 - Pyridoxine in Preventing Hand-Foot Syndrome Caused by Capecitabine in Patients With Cancer Phase 3
Completed NCT02625415 - The Topical Application of Vitamin B6 in Palmar-Plantar Erythrodysesthesia N/A
Active, not recruiting NCT00559858 - Pyridoxine in Preventing Hand-Foot Syndrome in Patients Who Are Receiving Capecitabine for Advanced Colorectal Cancer or Breast Cancer Phase 3
Terminated NCT00751101 - Nicotine Patches in Reducing Hand-Foot Syndrome in Patients Who Are Receiving Capecitabine For Metastatic Breast Cancer Phase 2
Completed NCT01100463 - Study of 0.1% Uracil Topical Cream (UTC) for the Prevention of Hand-Foot Syndrome Phase 1/Phase 2