Can a finger sensor perfectly measure pain during heart surgery?
NCT ID NCT06817005
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial tests whether a finger sensor, called the NOL index, can reliably measure pain signals during heart bypass surgery. The sensor tracks several body signals to help doctors give the right amount of pain medication. The study involves 50 adults undergoing this type of surgery. The main goal is to see if the sensor works without losing signal during the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- NOL index monitoring device (PMD200)
- What this could lead to
- If the NOL index works reliably during heart surgery, it could help doctors tailor pain medication precisely, reducing both pain and opioid side effects.
- What could go wrong
- This is a small feasibility study, so results may not apply broadly. The sensor might lose signal during surgery, and it's unclear if it improves outcomes.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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50 people
The number who actually took part.
- Started
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Mar 2025
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * adult patients * patients undergoing on-pump cardiac surgery * specific cardiac procedure : coronary artery bypass grafting Exclusion criteria: * patients with preoperative cardiac arrhythmia * patients with a cardiac pacemaker * emergency cardiac surgical procedure * peripheral artery disease stage 2 * patients in shock prior to the cardiac surgery : mean arterial pressure 65mmHg with vasopressors * persons participating in another interventional research * patient refusal
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Service d'Anesthésie Réanimation Cardiovasculaire
Strasbourg, 67000, France
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