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NCT01037595 Clinical Trial

Effect of Turmeric on Pruritus in Hemodialysis Patients

End Stage Renal Failure Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01037595
Other study ID # 3441
Secondary ID
Status Completed
Phase Phase 0
First received December 22, 2009
Last updated May 12, 2013
Start date September 2010
Est. completion date December 2010

Study information
Verified date May 2013
Source Shiraz University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority Iran: Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see whether turmeric can be effective in treatment of pruritus in hemodialysis patients.

Description:

pruritus is a common in hemodialysis patients and many treatment recommended for it . as turmeric has anti-inflammatory , anti-cytokine and anti-oxidant effect it may effective in treatment of uremic pruritus. thus we compared turmeric with placebo in this study

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date December 2010
Est. primary completion date October 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Hemodialysis for more than 3 months

- More than 18 years old

- Pruritus

Exclusion Criteria:

- Use other treatment for pruritus

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• turmeric
turmeric 500 md tid orally for 8 weeks
• placebo
placebo 3 time orally for 8 weeks
• turmeric
500 mg tid orally for 8 weeks

Locations
Country Name City State
Iran, Islamic Republic of Shiraz University Hemodialysis Center Shiraz Fars

Sponsors (1)
Lead Sponsor Collaborator
Shiraz University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary improvement in pruritus 6 mo Yes
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