Preventing nasal injuries in preterm infants on respiratory support
Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support
This study tests if special training for NICU nurses can help prevent nose injuries in preterm babies who need breathing support.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 30 (estimated) |
| Ages | 30 Weeks to 37 Weeks |
| Sex | All |
| Sponsor | Kafrelsheikh University Academic / other |
| Locations | 1 site (Kafr ash Shaykh, Kafr el-Sheikh Governorate) |
| Trial ID | NCT06642285 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of implementing evidence-based practices to prevent nasal pressure injuries in preterm neonates receiving non-invasive respiratory support. Over a week, NICU nursing staff will undergo education sessions focused on these guidelines. Preterm neonates will be randomly assigned to either a control group receiving standard care or a study group receiving targeted interventions. Data on the neonates' characteristics and clinical outcomes will be collected to assess the impact of these practices.
Who should consider this trial
Good fit: Ideal candidates are preterm neonates aged 30 to 37 weeks receiving non-invasive respiratory support.
Not a fit: Patients not receiving non-invasive respiratory support or those with prior nasal trauma or congenital abnormalities may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce the incidence of nasal pressure injuries in vulnerable preterm infants.
How similar studies have performed: While similar studies have explored interventions for preventing pressure injuries, this specific approach is novel in the context of preterm neonates.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Preterm neonates receiving NIRS * whose gestational ages ranges between 30 and 37 weeks, and both genders Exclusion Criteria: * all preterm neonates not receiving NIRS, * have prior nasal trauma caused by tracheal intubation * or Infants exhibiting evidence of nasal damage during the NIRS procedure, * have upper respiratory abnormalities. * preterm neonates who have undergone any type of surgery and had life-threatening congenital abnormalities.
Where this trial is running
Kafr ash Shaykh, Kafr el-Sheikh Governorate
- Kafrelsheikh University — Kafr ash Shaykh, Kafr el-Sheikh Governorate, Egypt (Recruiting)
Study contacts
- Principal investigator: Eman W Wardany, ass. professor — pediatric nursing department, faculty of nursing kafrelsheikh univeristy
- Study coordinator: Eman W abdelaal, Ass. Professor
- Email: eman_wardany_2014@nur.kfs.edu.eg
- Phone: 01065407334
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.