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Effect of ANI on Intraoperative Opioid Consumption

NCT05106452 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2021-11-11

No results posted yet for this study

Summary

The aim of the study is to compare the analgesic nociception index (ANI), which is used to determine the dose of analgesic agent needed in the intraoperative period, with the conventional method in patients with erector spinae block who underwent gynecological surgery under general anesthesia.

Conditions

  • Analgesia
  • Nociceptive Pain
  • Nerve Block
  • Pain

Sponsors & Collaborators

  • Zeynep Koc

    collaborator UNKNOWN

  • Zonguldak Bulent Ecevit University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-10-20
Primary Completion
2023-02-28
Completion
2023-05-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

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 NCT05106452 on ClinicalTrials.gov