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Clinical Trial Summary

using a biased-coin design up-down sequential method, different concentration of lidocaine will be used for popliteal block After 45 successful block (positive response), the data will be used to calculate the minimum lidocaine concentration that can result in successful popliteal block in 90% of patients


Clinical Trial Description

The response of a patient determined the lidocaine concentration given to the next patient (a biased-coin design up-down sequential method). If a patient had a negative response, the lidocaine concentration was increased by 0.1% w/v in the next patient. If a patient had a positive response, the next patient was randomized to receive the same lidocaine concentration (with probability of 0.89), or to receive a concentration 0.1% w/v less (with probability of 0.11). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03613974
Study type Interventional
Source Healthpoint Hospital
Contact
Status Not yet recruiting
Phase Phase 4
Start date December 15, 2018
Completion date March 31, 2019

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