|
Main
|
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
|
Register:
|
ClinicalTrials.gov |
|
Last refreshed on:
|
16 December 2017 |
|
Main ID: |
NCT02932670 |
|
Date of registration:
|
12/10/2016 |
|
Prospective Registration:
|
No |
|
Primary sponsor: |
|
|
Public title:
|
Minimum Effective Volume of Lidocaine Costoclavicular Brachial Plexus Block
|
|
Scientific title:
|
Minimum Effective Volume of Lidocaine for Ultrasound-Guided Costoclavicular Infraclavicular Brachial Plexus Block |
|
Date of first enrolment:
|
October 2016 |
|
Target sample size:
|
60 |
|
Recruitment status: |
Completed |
|
URL:
|
https://clinicaltrials.gov/show/NCT02932670 |
|
Study type:
|
Interventional |
|
Study design:
|
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Triple (Participant, Care Provider, Outcomes Assessor).
|
|
Phase:
|
N/A
|
|
|
Countries of recruitment
|
|
Canada
| | | | | | | |
|
Contacts
|
|
Name:
|
De QH Tran, MD |
|
Address:
|
|
|
Telephone:
|
|
|
Email:
|
|
|
Affiliation:
|
McGill University Health Center |
| | |
|
Key inclusion & exclusion criteria
|
Inclusion Criteria:
- age between 18 and 70 years
- American Society of Anesthesiologists classification 1-3
- body mass index between 20 and 30
Exclusion Criteria:
- adults who are unable to give their own consent
- pre-existing neuropathy (assessed by history and physical examination)
- coagulopathy (assessed by history and physical examination and, if deemed clinically
necessary, by blood work up i.e. platelets= 100, International Normalized Ratio= 1.4
or partial prothrombin time = 50)
- renal failure (assessed by history and physical examination and, if deemed clinically
necessary, by blood work up i.e. creatinine= 100)
- hepatic failure (assessed by history and physical examination and, if deemed
clinically necessary, by blood work up i.e. transaminases= 100)
- allergy to local anesthetics
- pregnancy
- prior surgery in the infraclavicular region
- chronic pain syndromes requiring opioid intake at home
Age minimum:
18 Years
Age maximum:
75 Years
Gender:
All
|
|
Health Condition(s) or Problem(s) studied
|
|
Upper Extremity Surgery
|
|
Intervention(s)
|
|
Other: costoclavicular nerve block
|
|
Primary Outcome(s)
|
|
success rate
[Time Frame: 0-30 min]
|
|
Secondary ID(s)
|
|
Montreal General Hospital
|
|
Source(s) of Monetary Support
|
|
Please refer to primary and secondary sponsors
|
|
Results
|
|
Results available:
|
|
|
Date Posted:
|
|
|
Date Completed:
|
|
|
URL:
|
|
|
|