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Efficacy of absorbable dressing foam on prevention of tracheostomy site infections

Efficacy of absorbable dressing foam on prevention of tracheostomy site infections

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205215426N5
Enrollment
80
Registered
2012-07-17
Start date
2012-06-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Tracheostomy site infections. Tracheostomy malfunction

Interventions

Intervention 1: Intervention group: The absorbable foams are used for dressing of theracheostomy site for 7 days. Intervention 2: Control Group: The normal gas are used for dressing of theracheostomy
Prevention
Intervention group: The absorbable foams are used for dressing of theracheostomy site for 7 days.
Control Group: The normal gas are used for dressing of theracheostomy site for 7 days.

Sponsors

Kerman University of Medical Sciences Research Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Eighteen to sixty Y/O patients; the patients with low GCSS (Glascow Coma Scale Score) because of head injury that this score, will not increase in up to 21 days, according to clinical information, diagnostic CT scan and Counseling with Neurologist; the Patients that undergoing tracheostomy at the first 3 days after ICU admission and all the Patients should receive the same antibiotics in ICU. Exclusion Criteria: the patients with Diabetes; Pneumonia; Renal failure; Hepatic failure; Chronic cardiopulmonary disorders; history of antibiotic therapy from last; clear infection signs in anterior neck; anterior neck burning and foam sensitivity.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Tracheostomy site infections. Timepoint: The culture samples from the tracheostomy site are prepared in 24, 72, 168 hours after tarcheostomy surgery. Method of measurement: The prepared culture samples from the tracheostomy site, sent to the laboratory as blind and followed up for result.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mehdi Ahmadi nejad

Kerman University of Medical Sciences

mehdia50@gmail.com+98 34 1223 5011

Outcome results

None listed

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