Clinical Trials Directory

Trials / Terminated

TerminatedNCT03365752

Chloroprocaine Spinal for Outpatient Knee Surgery

A Comparison Study to Facilitate Earlier Discharge: Spinal Versus General Anesthesia for Outpatient Knee Surgeries, a Randomized Controlled Study

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Hospital for Special Surgery, New York · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Outpatient knee surgeries with duration of less than one hour pose a challenge to the use of spinal anesthesia given that traditional agents remain in effect for 2-3 hours, thus creating a mismatch between length of surgery and anesthetic resolution. The investigators hypothesize that the use of chloroprocaine can combine the benefits of a short spinal anesthetic while avoiding the side effects of a general anesthetic, thus promoting earlier discharge.

Conditions

Interventions

TypeNameDescription
DRUGChloroprocaineA spinal anesthetic with 2% chloroprocaine (2cc or 40 mg) will be performed
DRUGMepivacaineA spinal anesthetic with 1.5% Mepivacaine (3cc or 45 mg) will be performed
DRUGGeneral AnestheticsGeneral anesthetics will be administered intravenously

Timeline

Start date
2018-06-24
Primary completion
2021-02-04
Completion
2021-02-04
First posted
2017-12-07
Last updated
2022-04-20
Results posted
2022-04-20

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03365752. Inclusion in this directory is not an endorsement.