Trials / Unknown
UnknownNCT04833296
Ropivacaine Use in Interscalene 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
This study aim to calculate the minimal effective ropivacaine concentration required achieve successful analgesic interscalene block in 90% of patients (MEAC90)
Detailed description
* Before induction of general anesthesia, all patients will receive interscalene block using 15ml of ropivacaine which concentration will be based on the response of the previous patient. * Based on biased-coin design up-down sequential method: if patient has pain free recovery, a successful block, the next patient will be randomized to receive either the same ropivacaine concentration or a concentration 0.01% w/v less. However, if he has an unsuccessful block, the next patient will receive a concentration 0.01% w/v higher. * 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 interscalene 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
- 2021-04-06
- Last updated
- 2021-04-06
Locations
1 site across 1 country: United Arab Emirates
Source: ClinicalTrials.gov record NCT04833296. Inclusion in this directory is not an endorsement.