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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

TypeNameDescription
DRUGRopivacaineall 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.