Viewing Study NCT06633861


Ignite Creation Date: 2025-12-24 @ 12:15 PM
Ignite Modification Date: 2026-01-03 @ 8:21 PM
Study NCT ID: NCT06633861
Status: COMPLETED
Last Update Posted: 2025-09-16
First Post: 2024-08-23
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Data Collection Study for RFP (Respiration From Plethysmogram)
Sponsor: Philips Clinical & Medical Affairs Global
Organization:

Study Overview

Official Title: Data Collection Study for RFP (Respiration From Plethysmogram)
Status: COMPLETED
Status Verified Date: 2025-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SAT+
Brief Summary: The study will be conducted in hospitalised patients who undergo spot-check monitoring of vital signs as part of their routine care.
Detailed Description: In an additional spot-check measurement procedure, the study will measure oxygen saturations through different Philips SpO2 finger sensors. Patients will wear a nasal cannula linked to a CO2 measuring device at the same time. The data from both devices will be used to design and improve algorithms for measurement of respiratory rate with the saturation probe and the Philips FAST pulse oximeter system. The study will include 50 adult patients and 25 pediatric patients.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: