Terminated NA INTERVENTIONAL 3-arm NCT04986163

Intraoperative Nociception Monitoring with Medstorm, Medasense and Anspec-pro During Total Intravenous Anesthesia

Randomized Controlled Trial for Intraoperative Nociception Monitoring with Medstorm, Medasense and Anspec-pro During Total Intravenous Anesthesia (TIVA) Using Propofol and Remifentanil

Sponsor: University Ghent

Conditions Pain Measurement

Interventions Non-invasive analgesia monitoring with ANSPEC-PRO monitor and MEDASENSE monitor Non-invasive analgesia monitoring with ANSPEC-PRO monitor and MEDSTORM monitor Non-invasive analgesia monitoring with MEDSTORM monitor and MEDASENSE monitor

Updated 5 times since 2021 Last updated: Sep 5, 2024 Started: Feb 3, 2021 Primary completion: Oct 25, 2022 Completion: Dec 13, 2022

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

Terminated

Technical issues

Other terminated trials from University Ghent

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A NA clinical study on Pain Measurement, this trial is terminated or withdrawn. The trial is conducted by University Ghent and has accumulated 5 data snapshots since 2021. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

5 versions recorded

Oct 2024 — Present [monthly]

Terminated NA
Sep 2024 — Oct 2024 [monthly]

Terminated NA
Jul 2024 — Sep 2024 [monthly]

Terminated NA
Feb 2023 — Jul 2024 [monthly]

Terminated NA

Status: Recruiting → Terminated
Sep 2021 — Feb 2023 [monthly]

Recruiting NA

First recorded

Feb 2021

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

University Ghent
University Hospital, Ghent

Data source: University Hospital, Ghent

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Ghent, Belgium