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Investigating the effect of Satoria hortensis on hemodialysis needling pai

Phase 2
Recruiting
Conditions
Hemodialysis.
Preparatory care for renal dialysis
Z49.0
Registration Number
IRCT20121031011341N12
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Patients with chronic kidney disease
Twice-weekly dialysis
History of dialysis through arteriovenous fistula for a minimum of 3 months
Full consciousness and sign a written consent for participation in the study

Exclusion Criteria

Allergy to herbal products
Skin injuries to the site of arteriovenous fistula
Consumption of oral sedatives in the past 6 hours or Local (arteriovenous fistula) pain medication in the past 24 hours
Diabetic or other types of neuropathy
Failure of the initial attempt to reach the arteriovenous fistula

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: immediately after needle insertion. Method of measurement: analog video scale (AVS).
Secondary Outcome Measures
NameTimeMethod
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