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Main
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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03486535 |
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Date of registration:
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27/03/2018 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Infraclavicular Block Properties in Diabetic Patients
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Scientific title:
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Ultrasound-Guided Infraclavicular Brachial Plexus Block Properties in Diabetic and Non-diabetic Patients: A Prospective Observational Study |
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Date of first enrolment:
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February 20, 2018 |
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Target sample size:
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60 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03486535 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Turkey
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Contacts
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Name:
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Emine A Salviz |
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Address:
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Telephone:
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Email:
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Affiliation:
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Istanbul University, Medical Faculty of Istanbul |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
Patients scheduled for arm, elbow, forearm, and hand surgery American Society of
Anesthesiologists (ASA) physical status I-IV No regional anesthesia contraindication
Exclusion Criteria:
Type 1 DM, Type 2 DM patients with only 'diet-controlled' therapy Difficulty with
understanding the block and follow-up instructions Significant neurologic disorders
Psychiatric or cognitive disorders History of substance abuse Acute and/or chronic opioid
use Local anaesthetic hypersensitivity or allergy
Age minimum:
40 Years
Age maximum:
80 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Diabetes Mellitus
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Pain, Postoperative
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Nerve Block Duration
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Intervention(s)
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Drug: Infraclavicular Brachial Plexus Blocks
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Primary Outcome(s)
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Sensory block duration
[Time Frame: 0-24 hours]
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Secondary Outcome(s)
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Motor block duration
[Time Frame: 0-24 hours]
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Pain (NRS) scores
[Time Frame: 0-48 hours]
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Sensory block onset time
[Time Frame: 0-30 minutes]
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Time-to-first pain
[Time Frame: 0-48 hours]
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Rescue analgesic consumption
[Time Frame: 0-48 hours]
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Motor block onset time
[Time Frame: 0-30 minutes]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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