New monitor may help doctors give just the right amount of pain medicine during surgery
NCT ID NCT05615441
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a special monitor that tracks pain signals during anesthesia can help doctors use less pain medicine during knee surgery. 54 adults having arthroscopic knee surgery were randomly assigned to receive either standard monitoring or the extra pain monitor. The goal was to see if the monitor led to lower pain medicine use and better pain control after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Analgesia Nociception Index monitor (device)
- What this could lead to
- If it works, this could help doctors give just the right amount of pain medicine during surgery, leading to better pain control and fewer side effects.
- What could go wrong
- This is a small, early-stage study with only 54 people. The monitor may not actually reduce pain medicine needs or improve recovery in a meaningful way.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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
-
54 people
The number who actually took part.
- Started
-
Jul 2023
- Finished
-
Nov 2025
- Lead sponsor
-
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
-
19 to 64 years
- Sex
-
Anyone
- Healthy volunteers
-
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 between 19 and 64 years of age, ASA class I\~III, scheduled for arthroscopic knee surgeryunder general anesthesia. Exclusion Criteria: Patient refusal, patients unable to read consent form, active URI or uncontrolled asthma, pneumonia, history of allergies to benzodiazepines, decreased liver or kidney function, heart failure of ejection fraction\<55%, pregnant or breastfeeding patients, history of substance abuse/addiction
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Adult patients aged 19-64, scheduled for elective arthroscopic knee surgery are added.
Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Yonsei University Health System, Severance Hospital
Seoul, South Korea