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Prevention study for Mechanical Ventilation Complication
Official title Effect of Implementing Evidence Based Practices on Prevention of Associated Nasal Pressure Injuries Among Preterm Neonates With Non-Invasive Respiratory Support
ClinicalTrials.gov ID: NCT06642285
What this study is testing
- What it's testing
- This study aims to evaluate the effect of implementing evidence based practices on prevention of associated nasal pressure injuries among preterm neonates with non invasive respiratory support
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 30 to 37. Healthy volunteers may be eligible.
You may be able to join if
- Preterm neonates receiving NIRS
- whose gestational ages ranges between 30 and 37 weeks, and both genders
You likely can't join if
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Kafr ash Shaykh, Kafr el-Sheikh Governorate, Egypt
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 30 weeks to 37 weeks. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Kafr ash Shaykh, Kafr el-Sheikh Governorate, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.