Clinical Trials Directory

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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

TypeNameDescription
DRUGRopivacaineall 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.