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The Effect of Phytochemicals on the treatment of Phlebitis

Not Applicable
Completed
Conditions
phlebitis.
Vascular complications following infusion, transfusion and therapeutic injection
Registration Number
IRCT2015061422738N1
Lead Sponsor
Deputy of Research and Technology, Birjand University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
Inclusion Criteria

I having an IV catheter, gauge No. 20 (with all catheters of an essentially single brand), age between 18-60 years old, hospitalization in the internal medicine ward for at least 72 hours, no allergy to the drugs and the wound dressing, lack of blood transfusion, systolic blood pressure between 90 to 180 mmHg, no diabetes, no skin disease in the area of phlebitis, no pregnancy or lactation, having at least one phlebitis symptom (pain, redness, irritation) around the area, no chemical or herbal oil use for treatment of the phlebitis during the study, no history of allergy to the plants containing Quercetin or Tannic acid, using upper limbs for catheterization, using aseptic conditions for catheterization
Exclusion criteria: patients discharged before three days, taking contraceptive drugs, patients with known comorbidities including hyper-coagulability states (e.g., anti-cardiolipin antibodies, anti-phospholipid antibodies, and vitamin C deficiency)

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Phlebitis. Timepoint: Before and 12 hours after treatment for 72 hours. Method of measurement: 4 degree visual phlebitis scale.
Secondary Outcome Measures
NameTimeMethod
Dermal side effects. Timepoint: 12 hours for 72 hours. Method of measurement: Observation.
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