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The effect of nano antimicrobial dressings on the healing of wound infections

Phase 2
Recruiting
Conditions
Infection following cesarean section.
Infection following a procedure
T81.4
Registration Number
IRCT20210705051790N1
Lead Sponsor
Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
100
Inclusion Criteria

Patients with evidence of localized cellulitis or wound redness or discharge from the incision cesarean section or hysterectomy
Informed consent

Exclusion Criteria

Patients with a history of skin allergies to nanoproducts
Patients with systemic symptoms suggestive of impending doom fever, chills or leukocytosis (more than 16 thousand) and need to be injected with antibiotics.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ague. Timepoint: At the time of hospitalization (average 2 to 3 days after surgery), 4 to 7 days after surgery, 2 weeks after discharge. Method of measurement: Question from the patient.;Infection. Timepoint: At the time of hospitalization (average 2 to 3 days after surgery), 4 to 7 days after surgery, 2 weeks after discharge. Method of measurement: Examination and observation by a physician.
Secondary Outcome Measures
NameTimeMethod
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