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Effect of chamomile versus placebo on first-degree pressure ulcer in patients hospitalized in IC

Phase 2
Recruiting
Conditions
Pressure ulcer.
Pressure ulcer
Registration Number
IRCT20120215009014N205
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
64
Inclusion Criteria

Age of 18 to 70 years
Hospitalized in ICU
Having first-degree pressure ulcer

Exclusion Criteria

A history of allergy or cutaneous hypersensitivity
Any hypersensitivity to chamomile

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of ulcer. Timepoint: On 4 and 7 days after intervention. Method of measurement: Through physical examination.
Secondary Outcome Measures
NameTimeMethod
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