Intrathecal Chloroprocaine for Lower Limb Arthroplasty

NCT05365074 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 65

Last updated 2022-05-09

No results posted yet for this study

Summary

This study evaluates the perioperative course in adult patients undergoing total or partial knee arthroplasty, or total hip arthroplasty under chloroprocaine spinal anesthesia.

Conditions

  • Lower Limb Arthroplasty Under Chloroprocaine Spinal Anesthesia

Interventions

DRUG

Chloroprocaine Injection

Spinal anesthesia with 50 mg of 1% Chloroprocaine

Sponsors & Collaborators

  • Hospices Civils de Lyon

    collaborator OTHER
  • Hôpital de la Croix-Rousse

    lead OTHER

Eligibility

Sex
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-01
Primary Completion
2021-12-31
Completion
2022-03-02

Countries

  • France

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 NCT05365074 on ClinicalTrials.gov