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Investigation of the Local Effect of Propolis Cream on The infection and the time of the occurrence

Not Applicable
Conditions
Condition 1: Phlebitis. Condition 2: infection.
Phlebitis and thrombophlebitis
Other bacterial infections of unspecified site
A49.8
Registration Number
IRCT20131228015965N14
Lead Sponsor
Rafsanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
76
Inclusion Criteria

Venous access for at least 72 hours,
The absence of skin and peripheral vascular diseases,
Healthy upper limb,
The absence of phlebitis in the anjection site,
No use of steroids, heparin, injectable nitroglycerin,
Age is more than 18 years old

Exclusion Criteria

Unwanted side effects
Any factor other than phlebitis that causes the patient to get out of the reach of 72 hours

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phlebitis. Timepoint: Every 12 hours to 72 hours. Method of measurement: Checklist for phlebitis symptoms.;Infection. Timepoint: After the end of the intervention. Method of measurement: CBC blood test.
Secondary Outcome Measures
NameTimeMethod
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