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| Name | Class |
|---|---|
| Hospices Civils de Lyon | OTHER |
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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 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 |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Chloroprocaine Injection | Drug | Spinal anesthesia with 50 mg of 1% Chloroprocaine |
|
| Measure | Description | Time Frame |
|---|---|---|
| Spinal anesthesia failure | proportion of patients with the necessity to convert initially planned spinal anesthesia into general anesthesia | Day 0 |
| Measure | Description | Time Frame |
|---|---|---|
| Hemodynamic instability | proportion of patients with >20% changes in blood pressure and ou heart rate comparing to baseline | Day 0 |
| Need for sedation | proportion of patients requiring intraoperative sedation for uncomfortable conditions |
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Inclusion Criteria:
Exclusion Criteria:
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Adult patients operated for total knee, unicompartment knee or anterior access hip arthroplasty under chloroprocaine spinal anesthesia in the period of years 2020 - 2021
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hopital de la Croix Rousse - Hospices Civils de Lyon | Lyon | 69004 | France |
IPD are protected by the French regulation and will not be shared
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| ID | Term |
|---|---|
| C004616 | chloroprocaine |
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| Day 0 |
| Surgical block duration | time of regression of sensitive and motor spinal block | Day 0 |
| PACU analgesia requirement | morphine equivalent requirement in PACU for the postoperative pain | Day 0 |
| Urinary retention | proportion of patients requiring urinary catheter | 24 hours |
| Postoperative nausea and vomiting | proportion of patients having nausea and vomiting | 24 hours |
| Length of stay in recovery room | Length of stay in recovery room | Day 0 |