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Surgical Intervention in Deep Sedation: No Pain or no Memory

NCT06963749 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 36

Last updated 2025-08-06

No results posted yet for this study

Summary

The goal of this observational study is to assess the levels of nociception in deeply sedated patients who need painful and short-duration surgical procedure.

The main question it aims to answer is to verify that the sedative protocols used in clinical practice are sufficiently effective also in terms of nociception.

Participants will deeply sedated and monitored with PMD-200™ to detect the nociception level (NOL Index).

Conditions

  • Pain, Acute
  • Surgical Procedure, Unspecified

Sponsors & Collaborators

  • ASL Novara

    lead OTHER_GOV

Principal Investigators

  • Davide Colombo, PhD · ASL Novara

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2025-01-31
Completion
2025-01-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06963749 on ClinicalTrials.gov