Intrathecal Chloroprocaine for Lower Limb Arthroplasty

NCT ID: NCT05365074

Last Updated: 2022-05-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

65 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2022-03-02

Brief Summary

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

Detailed Description

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This study evaluates the failure rate of spinal anesthesia, the duration of surgical anesthesia, the needs for complementary intraoperative analgesia, the time for recovery, the incidence of urinary retention, postoperative nausea and vomiting, and length of stay in the recovery room in patients operated for knee or hip arthroplasty under spinal anesthesia with chloroprocaine 50 mg.

Conditions

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Lower Limb Arthroplasty Under Chloroprocaine Spinal Anesthesia

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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chloroprocaine anesthesia for arthroplasty

patients having predicted uncomplicated surgery for total or unicompartment knee arthroplasty of anterior access total hip arthroplasty, operated under spinal anesthesia with 50 mg of chloroprocaine

Chloroprocaine Injection

Intervention Type DRUG

Spinal anesthesia with 50 mg of 1% Chloroprocaine

Interventions

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Chloroprocaine Injection

Spinal anesthesia with 50 mg of 1% Chloroprocaine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* adult patients
* with spinal anesthesia using 50 mg of chloroprocaine
* operated for total knee, unicompartment knee or anterior access hip arthroplasty
* in the period of years 2020 - 2021

Exclusion Criteria

* expressed disagreement to to participate after receiving information notice
Eligible Sex

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role collaborator

Hôpital de la Croix-Rousse

OTHER

Sponsor Role lead

Responsible Party

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Mikhail Dziadzko, MD, PhD

Senior physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hopital de la Croix Rousse - Hospices Civils de Lyon

Lyon, , France

Site Status

Countries

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France

Other Identifiers

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CSE-HCL 22_729

Identifier Type: -

Identifier Source: org_study_id

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