Skip to content

Comparison of the effect of two methods of primary washing of the area disinfected with brown betadine with 70% alcohol and normal saline on the incidence and severity of postoperative wound infection

The Comparison of the Incidence and Severity of Wound Infection to 2 Methods of Primary Prep Washing with 70% Alcohol and Normal Saline in Patients Undergoing Orthopedic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160301026861N3
Enrollment
190
Registered
2023-04-24
Start date
2020-04-08
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary prep area of patients candidates for elective orthopedic surgery of the upper limbs.

Interventions

Intervention 1: Intervention group: The surgical site must be completely shaved. The surgical area will be prepped with 5.7% betadine brown diluted with normal saline for three minutes. After the init

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patient is a volunteer for elective orthopedic surgery of the upper limb The patient is a volunteer to participate in the research The hair in the surgical area must be shaved before the operation The body mass index of the patient is less than 30

Exclusion criteria

Exclusion criteria: There should be no skin damage in the surgical area due to trauma The patient does not have any underlying diseases or skin allergies The patient does not have burns or previous surgery in the prep area The patient does not have vascular problems in the organ under surgery The patient does not have diseases related to the immune system and infectious diseases The patient does not have digestive or blood diseases

Design outcomes

Primary

MeasureTime frame
The incidence of wound infection after surgery with a score higher than ten from the wound evaluation and the absence of wound infection with a score lower than 10 will be measured by the ASEPSIS INDEX tool after orthopedic surgery. Timepoint: It will be measured once. The symptoms of wound infection will be monitored from the time after surgery until two weeks after discharge from the hospital, and on the 14th day after discharge, the scores obtained from the Asepsis index tool will be collected. Method of measurement: Based on the ASEPSIS INDEX tool, evaluation of wound healing after surgery including; Complementary antibiotic therapy (0-10 points), redness of the wound at the surgical site (0-5 points), serous discharge from the surgical site (0-5 points), deep disintegration of the wound (0-10 points), culture from the wound site and isolation of bacteria ( 0-10 points) Wound debridement under general anesthesia (0-10 points), drainage of purulent wound secretions under local anesthesia, purulent exudate (0-10 points), hospitalization for more than 14 days (0-5 points). The maximum score will be 70 and the minimum score will be zero. A score less than ten means complete healing of the wound and no wound infection. A score higher than ten means wound infection.;The severity of wound infection after surgery will be determined based on the ASEPSIS INDEX standard tool. Based on this tool, a score of 0-10 indicates complete healing of the wound, a score of 11-20 indicates impaired wound healing, a score of 21-30 indicates partial wound infection, a score of 31-40 indicates moderate wound infection, and a score greater than 40 indicates severe wound infection. Timepoint: It will be measured once. The symptoms of wound infection will be monitored from the time after surgery until two weeks after discharge from the hospital, and on the 14th day after discharge, the scores obtained from the Asepsis index tool will be collected. Method of measurement: In this study, the a

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJamal Seidi

Sanandaj University of Medical Sciences

jamal.seidi@muk.ac.ir+98 87 3366 0095

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026