Trials / Unknown
UnknownNCT04834440
Ropivacaine Use in Femoral Nerve Block; What is the Minimal Effective Analgesic Concentration (MEAC 90)
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 45 (estimated)
- Sponsor
- Healthpoint Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to determine the minimal effective ropivacaine concentration required to provide adequate analgesic femoral nerve block in 90% of patients (MEAC90)
Detailed description
* Before induction of GA, all patients will receive sciatic, obturator, lateral femoral cutaneous and femoral nerve blocks. * The femoral nerve block will be performed using 15ml of ropivacaine which concentration relied on the response of the previous patient. * Based on biased-coin design up-down sequential method: when a patient has a negative response, the next patient will receive a concentration 0.01% w/v higher. However if he has a positive response, the next patient will be randomized to receive either the same ropivacaine concentration or a concentration 0.01% w/v less. * Patients with pain free recovery will be considered to have positive response. * Patients' responses will be analyzed to calculate the MEAC90
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine | all patients will receive femoral nerve block using same volume of ropivacaine but in different concentrations |
Timeline
- Start date
- 2021-05-01
- Primary completion
- 2021-09-30
- Completion
- 2021-09-30
- First posted
- 2021-04-08
- Last updated
- 2021-04-08
Locations
1 site across 1 country: United Arab Emirates
Source: ClinicalTrials.gov record NCT04834440. Inclusion in this directory is not an endorsement.