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Evaluation of moxifloxacin effevtiveness in wound healing

Phase 3
Conditions
Wounds from the site of general surgery.
Registration Number
IRCT20181208041882N5
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
80
Inclusion Criteria

Patients who have undergone general surgery
Patients over 18 years old

Exclusion Criteria

Diabetes
Liver failure
Renal failure
Epilepsy
Rheumatoid Arthritis
Heart failure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Review of the Redness, Edema, Ecchymosis, Discharge, Approximation index. Timepoint: Days 0, 1, 3 and 5 after surgery. Method of measurement: Observational.
Secondary Outcome Measures
NameTimeMethod
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