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
| Type | Name | Description |
|---|---|---|
| DRUG | Chloroprocaine | A spinal anesthetic with 2% chloroprocaine (2cc or 40 mg) will be performed |
| DRUG | Mepivacaine | A spinal anesthetic with 1.5% Mepivacaine (3cc or 45 mg) will be performed |
| DRUG | General Anesthetics | General 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03365752. Inclusion in this directory is not an endorsement.