Trials Sponsors Conditions Drugs Pricing

Conditions

Cardiac Surgery Subjects

Keywords

pain thresholdintra operative opioid consumptionalgometer

Outcome Measures

Primary Outcomes (1)

Correlation between the pressure pain threshold and the consumption of opioid during and after the surgery
After the measure of the minimal pain threshold the day before the surgery, the investigators look at the quantity of Remifentanil which has been given to the patient during the surgery. Then they will look for a correlation
From enrollment to the end of opioid administration during hospital stay, up to 6 days after the enrollment

Secondary Outcomes (1)

Correlation between the pain threshold and the consumption of morphine during the post-operative time
From enrollment to the end of opioid administration during hospital stay, up to 6 days after the enrollment

Study Arms (1)

pain threshold arm

OTHER

In this arm, patients get a measure of their minimal pain threshold in the preoperative time, that is the only intervention they get in addition of the classic care support

Device: Measure of the minimal pain threshold with an algometer

Interventions

Measure of the minimal pain threshold with an algometerDevice

The measure of the minimal pain threshold is taken the day before the cardiac surgery

pain threshold arm

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Sexall

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

ASA 3 patients with scheduled cardiac surgery by thoracotomy or sternotomy

You may not qualify if:

Sponsors & Collaborators

Université Libre de Bruxelles
Otherlead

Study Sites (1)

Erasme Hospital

Brussels, Anderlecht, 1070, Belgium

RECRUITING

Dr. IONUT TABOLCEACONTACT+32 488 72 00 46 Ionut.tabolcea@hubruxelles.be

NATHAN ASSERAFCONTACT+33 6 95 95 13 61 nathan.asseraf@ulb.be

IONUT TABOLCEA, DoctorPRINCIPAL INVESTIGATOR

Study Officials

IONUT TABOLCEA, Doctor
Erasme University Hospital
PRINCIPAL INVESTIGATOR

Central Study Contacts

IONUT TABOLCEA, Doctor

CONTACT

+32 488 72 00 46 Ionut.tabolcea@hubruxelles.be

NATHAN ASSERAF

CONTACT

+33695951361

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: TREATMENT
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: PRINCIPAL INVESTIGATOR
PI Title: Medicine student

Study Record Dates

First Submitted

March 27, 2026

First Posted

April 7, 2026

Study Start

January 24, 2026

Actual (reported)

Primary Completion

December 15, 2026

Estimated

Objective Measurement of the Mechanical Pain Threshold With an Algometer for Predicting Intraoperative Opioid Consumption in Patients Who Will be Operate by Thoracotomy and Sternotomy in Cardiac Surgery

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

pain threshold arm

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

Data Sharing

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Study Arms (1)

pain threshold arm

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Study Officials

Central Study Contacts

Study Design

Study Record Dates

Data Sharing

Source record

Locations