uremic pruritus. Other pruritus
Conditions
Interventions
Intervention 1: Control group :
Received no specific intervention . Intervention 2: Intervention group :
From sweet almond oil made by Iranian Barij Essence pharmaceutical company with License registr
Treatment - Drugs
Intervention group :
From sweet almond oil made by Iranian Barij Essence pharmaceutical company with License registration number “ s – 90 – 050 “ was used. This oil is contained from 77% oleic acid a
Sponsors
Yasuj University of Medical Science
Eligibility
Sex/Gender
All
Age
19 Years to 87 Years
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Uremic 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZahra Mehri
Yasuj University of Medical Science
Outcome results
None listed