Phase
Condition
N/ATreatment
Chlorhexidine
Povidone-Iodine
Povidone-Iodine and Chlorhexidine Antiseptic Treatment for Surgical Wound Management
Clinical Study ID
Ages 18-45 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Elderly patients undergoing surgical procedures resulting in iatrogenic wounds (surgical wounds of various specialties, such as abdominal, orthopedic,cardiovascular, etc.).
Availability for follow-up during the postoperative period, ensuring attendance atmedical check-ups for the evaluation of healing and prevention of infections.
Ability to provide informed consent, understanding the objectives, risks andbenefits of the study.
Absence of previous infections at the surgical site, ensuring that the wounds arerecent and derived from the current surgical procedure.
Exclusion
Exclusion Criteria:
Known allergies or hypersensitivity to povidone iodine or chlorhexidine, to avoidrisks of serious adverse reactions.
Immunocompromised patients, such as those with advanced HIV, on immunosuppressanttreatment, or with decompensated chronic diseases (poorly controlled diabetes,kidney failure, etc.), due to increased susceptibility to infections and alteredhealing.
Patients with active infections or infected wounds prior to surgery, to avoidbiasing the results by pre-existing infections.
Pregnancy or breastfeeding, due to safety considerations and the possible alterationof healing and immunity processes during these stages.
Use of other antiseptics or topical treatments at the wound site that may interferewith the efficacy of povidone iodine or chlorhexidine.
Patients with known wound healing disorders (such as autoimmune diseases orhematological disorders), which may affect the results in terms of healing time andquality.
Study Design
Connect with a study center
María Juana Millán Reyes
Jaén, 23007
SpainSite Not Available
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