Status:

COMPLETED

Analgesic Effect of Ropivacaine Combined With Hydromorphone for CSEA After Total Knee Arthroplasty

Lead Sponsor:

Second Hospital of Jilin University

Conditions:

Postoperative Analgesia

Eligibility:

All Genders

55-80 years

Phase:

NA

Brief Summary

The aim of this study is to investigate the continuous analgesic effect and side effects of ropivacaine combined with hydromorphone for combined spinal-epidural anesthesia(CSEA) after total knee arthr...

Detailed Description

For patients undergoing total knee arthroplasty, different spinal anesthesia drugs were injected in the two groups. The spinal anesthetic drugs injected in the hydromorphone group were hydromorphone 5...

Eligibility Criteria

Inclusion

  • Age between 55 and 80 years old.
  • ASA grade I to III.
  • BMI:20-29kg/m2.
  • No recent use of sedatives, opioids, or other analgesics.
  • There was no contraindication of spinal anesthesia, severe dysfunction of heart, lung and other important organs or serious systemic diseases.
  • Patients were willing to participate in the study and signed the informed consent.

Exclusion

  • The patient has mental illness or cannot cooperate with the completion of spinal anesthesia.
  • The patient had a history of spinal surgery and spinal deformity.
  • Patients had a history of opioid intolerance or adverse reactions.
  • puncture site infection, coagulopathy or recent use of anticoagulant drugs.
  • History of allergy to local anesthetics.
  • Failed puncture.
  • Unable to cooperate to complete the research process.

Key Trial Info

Start Date :

October 27 2022

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 30 2023

Estimated Enrollment :

136 Patients enrolled

Trial Details

Trial ID

NCT06205199

Start Date

October 27 2022

End Date

November 30 2023

Last Update

January 24 2024

Active Locations (1)

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Second Hospital of Jilin University

Changchun, Jilin, China