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Impact of Perioperative Antibiotic Use on Surgical Scarring

Perioperative Antibiotic Use and Its Impact on Postoperative Scarring: A Retrospective Study

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07741591
Acronym
PASS
Enrollment
5000
Registered
2026-08-03
Start date
2026-08-03
Completion date
2026-08-15
Last updated
2026-08-03

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

Conditions

Postoperative Scar, Surgical Scar

Keywords

Perioperative Antibiotics, Surgical Scar, Postoperative Scar, Scar Assessment, Visual Analogue Scale

Brief summary

This retrospective observational cohort study will evaluate whether perioperative antibiotic use is associated with long-term surgical scar outcomes. The study will include adult patients who underwent body surface surgery at Nanfang Hospital between January 1, 2005 and January 1, 2025 and have available surgical, medication, and scar-related clinical records. The study will not assign participants to any treatment. Researchers will review existing medical records, perioperative antibiotic exposure, surgical characteristics, complications, and scar assessments or photographs. Scar outcomes will be assessed using modified visual analogue scale scores, scar width, scar type, and scar-related complications.

Interventions

OTHERPerioperative Antibiotic Exposure

Patterns of perioperative antibiotic use documented in existing medical records, including timing, indication, antibiotic type, duration, frequency, and route of administration. No antibiotic treatment will be assigned or provided by the study.

Sponsors

Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older. * Underwent body surface surgery at Nanfang Hospital between January 1, 2005 and January 1, 2025, with a linear surgical incision scar. * Presented to the Department of Plastic Surgery at Nanfang Hospital for surgical scar-related care. * Had no medical encounter record at Nanfang Hospital from January 1, 2025 to the time of study screening. * Available clear surgical records and perioperative medication records.

Exclusion criteria

* Known tendency for pathological scarring or scar constitution. * History of chronic skin disease in the surgical area, such as psoriasis or eczema. * Uncontrolled diabetes mellitus, malnutrition, hypoalbuminemia, or long-term use of immunosuppressive agents or glucocorticoids. * Target scar received any scar-specific treatment after surgery, such as laser therapy, radiotherapy, drug injection, or surgical revision.

Design outcomes

Primary

MeasureTime frameDescription
Overall Scar Appearance Score Assessed Using a Modified Visual Analogue ScaleScar photographs were taken during postoperative clinical follow-up, with an overall range from 3 months to 20 years after surgery. Given the wide span, the assessments will be stratified and reported according to the actual time of photography, for examOverall scar appearance will be evaluated from scar photographs by three blinded physicians or trained study personnel using a modified visual analogue scale. Scores range from 1 to 10, with 1 indicating appearance similar to normal skin and 10 indicating the worst imaginable scar appearance.

Secondary

MeasureTime frameDescription
Scar Color Score Assessed Using a Modified Visual Analogue ScaleScar photographs were taken during postoperative clinical follow-up, with an overall range from 3 months to 20 years after surgery. Given the wide span, the assessments will be stratified and reported according to the actual time of photography, for examScar color will be evaluated from scar photographs by three blinded physicians or trained study personnel using a modified visual analogue scale. Scores range from 1 to 10, with lower scores indicating color more similar to normal skin and higher scores indicating worse scar color.
Scar Texture Score Assessed Using a Modified Visual Analogue ScaleScar photographs were taken during postoperative clinical follow-up, with an overall range from 3 months to 20 years after surgery. Given the wide span, the assessments will be stratified and reported according to the actual time of photography, for examScar texture will be evaluated from scar photographs by three blinded physicians or trained study personnel using a modified visual analogue scale. Scores range from 1 to 10, with lower scores indicating texture more similar to normal skin and higher scores indicating worse scar texture.
Scar WidthScar photographs were taken during postoperative clinical follow-up, with an overall range from 3 months to 20 years after surgery. Given the wide span, the assessments will be stratified and reported according to the actual time of photography, for examScar width will be calculated from scar photographs by outlining the scar boundary and using ImageJ to measure scar area and scar length. Scar width will be calculated as scar area divided by scar length.
Scar-Related ComplicationsPostoperative days 0 to 30 (inclusive). The timing of each complication was determined from medical records.Scar-related complications will be identified from medical records and scar assessments, including wound dehiscence, suture reaction, necrosis, hematoma, infection, persistent itching, persistent pain, and sensory abnormalities.

Countries

China

Contacts

CONTACTGaofeng Wang, Principal Investigator
Wenzhenli0526@163.com+86 13242749806

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 4, 2026