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Triclosan-antibacterial Sutures Efficacy on the Incidence of Surgical Site Infection in Clean-contaminated Wounds

Triclosan-antibacterial Sutures Efficacy on the Incidence of Surgical Site Infection in Clean-contaminated Wounds; Multi-center, Double Blind, Randomized Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04256824
Enrollment
430
Registered
2020-02-05
Start date
2020-02-05
Completion date
2024-01-30
Last updated
2023-09-06

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

Conditions

Surgical Site Infection, Surgical Wound, Surgical Wound Infection

Brief summary

Comparing the incidence of SSI in cases using coated Polyglactin 910 suture with Triclosan and cases using Polyglactin 910 suture without Triclosan in clean-contaminated wound surgery

Detailed description

Comparing the incidence of surgical site infection (SSI) in cases using coated Polyglactin 910 suture with Triclosan and cases using Polyglactin 910 suture without Triclosan in clean-contaminated wound surgery. Also, comparing the post hospital stay.

Interventions

Coated Polyglactin 910 with Triclosan (coated vicryl plus)

DRUGVicryl

Coated Polyglactin 910 without Triclosan (vicryl)

Sponsors

Misr University for Science and Technology
CollaboratorOTHER
Al Safwa Hospital
CollaboratorUNKNOWN
Al Zohour Hospital
CollaboratorUNKNOWN
Al-Menia Univeristy Hospital
CollaboratorUNKNOWN
MSKMC Univeristy Hospital
CollaboratorUNKNOWN
ClinAmygate
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

randomized-controlled study

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age: 18-75 * clean-contaminated wound surgery

Exclusion criteria

* Patient has immunodeficiency disorder. * Patient receiving anti-cancer / immunosuppressive therapy. * Patients with established pre-operative infection whether community acquired or hospital acquired either at / remote from the operative site.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of surgical site infection30 daysIncidence of surgical site infection within 30 days

Secondary

MeasureTime frameDescription
Hospital stay30 daysduration of hospital stay

Countries

Egypt

Contacts

Primary ContactEmad R Issak, Diploma
dr.emad.r.h.issak@gmail.com00201272228989

Outcome results

None listed

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