Non-Invasive Pressure Monitor for Neonates & Infants at Risk of Developing Hydrocephalus
A legfontosabb adatok
- Hol
- Indianapolis (Egyesült Államok)A helyszín megnézése
Helyszínek itt: Egyesült Államok
- Riley Hospital for ChildrenIndianapolis, Egyesült ÁllamokNo longer taking part
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Indiana University
- Azonosító
- NCT06310213
- A regiszteradat frissítve
- 2025. október 8.
- Eredeti leírás
The goal of this clinical trial is to test a modified smart soft contact lens in neonates and infants at risk of developing hydrocephalus. The main questions it aims to answer are:A teljes eredeti leírásKevesebb
The goal of this clinical trial is to test a modified smart soft contact lens in neonates and infants at risk of developing hydrocephalus. The main questions it aims to answer are:
* Can the device distinguish between intracranial pressure variations in neonates and infants diagnosed with hydrocephalus and those without * Can the device compare pressure dynamics between pre- and post-operative periods in neonates and infants who undergo surgical treatments Participants will undergo standard of care evaluations for hydrocephalus (anterior fontanelle assessment and head circumference measurement) and wear the device during standard of care evaluation; pre- and post- ventricular reservoir taps, as applicable; and/or pre- and post-operatively, as applicable.
Bevonási feltételek: Being monitored for hydrocephalus, or healthy controls.
Kizáró feltételek: Known hypersensitivity to materials used in the contact lens and/or adhesive; Other conditions deemed relevant by the medical team; Open/closed wounds at/near the anterior fontanelle; Anterior fontanelle is closed.