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The effect of sweet almond oil on the pruritus and quality of life in hemodialysis patients

Phase 2
Conditions
uremic pruritus.
Other pruritus
Registration Number
IRCT2014121520313N1
Lead Sponsor
Yasuj University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
42
Inclusion Criteria

participant is known cace of Chronic Renal Disease and under hemodialysis therapy at least 6months; suffering from pruritus to arise Chronic Renal Disease at least 2weeks; participant has only suffering from Chronic Renal Disease and has not suffering from known cace of pruriginous dermal disease; participant has age more than 18years; participant is healthy Psychologically; participant has not conscious disorder; participant has not speaking disorder; participant has not hearing disorder; participant has not seeing disorder; participant has informed tendency to participate in study.

Exclusion criteria:
participant express noninclination to participate in study in any stage of study; participant do not to apply sweet almond oil during the study; participant dies during the study; participant emigrates from study invironment during the study; participant receive renal transplant during the study; participant being under long term treatment with antihistamines or other pruritus sedative Medications during the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
remic pruritus. Timepoint: one week pre-intervention , the end of the first week after intervention and the end of the second week after intervention. Method of measurement: severity scale questionnaire.;Itchy quality of life. Timepoint: one week pre-intervention , the end of the first week after intervention and the end of the second week after intervention. Method of measurement: Itchy quality of life questionnaire.
Secondary Outcome Measures
NameTimeMethod
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