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NCT06832553

The Effect of Surgical Incision Drep Use in Endotracheal Tube Fixation

Recruiting now NA Last updated 14 March 2025
What this trial tests

NA trial testing surgical incision drep in Preterm in 110 participants. Currently enrolling.

Timeline
15 October 2024
Primary endpoint
15 May 2025
15 July 2025

Quick facts

Lead sponsorHasan Kalyoncu University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment110
Start date15 October 2024
Primary completion15 May 2025
Estimated completion15 July 2025
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Hasan Kalyoncu University

Who can join

Adults 28 Weeks to 34 Weeks, any sex, with Preterm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

It is aimed to minimise both unplanned extubation and skin damage with the surgical incision drep that we will use to fix the endotracheal tube in neonatal preterm infants and to reduce the complications that may develop due to these events. In addition, it is aimed to evaluate the relationship between these parameters by using devices measuring skin moisture, skin pH and Neonatal Skin Condition Assessment Scale in experimental and control groups.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Preterm

Currently open trials in the same condition.

Other Hasan Kalyoncu University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06832553.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing