Non-invasive, Real-time Anesthetic Drug-monitoring System

• Conditions: Anesthesia

• Registration Number: NCT02776020
• Lead Sponsor: Rambam Health Care Campus

Brief Summary

The aim of this study is to determine efficacy of the "CorrecDose" device to continuously and non-invasively follow the changes in propofol concentrations in the participants' blood.

Detailed Description

Not available

Study Timeline

• Status Verified: 2016-05
• Study First Submitted: 2016-05-09
• Study First Submitted QC: 2016-05-15
• Last Update Submitted: 2016-05-15
• Study First Posted: 2016-05-18
• Last Update Posted: 2016-05-18
• Study Start: 2016-06
• Primary Completion: 2016-12
• Study Completion: 2017-02

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: Female
• Target Recruitment: 30

Inclusion Criteria

• Women who have signed Informed consent form
• Women undergoing Trans vaginal ovum retrieval (TVOR) for invitro fertilization (IVF) and will be sedated with propofol administered intravenos (IV)

Exclusion Criteria

• Women with background diseases
• Women with chronic use of drug and medication
• Women with peripheral blood vessels problems
• Women with high blood pressure
• Women with body mass index (BMI) score over 35 or less than 18

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Changes in Propofol Blood Levels	Half hour	Graphic display on monitor of real-time changes