- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04857216
Comparison of the Block Characteristics of USG Guided Costoclavicular and Infraclavicular Block With the Perfusion Index
Comparison of the Block Characteristics of Ultrasound Guided Costoclavicular and Infraclavicular Block With the Perfusion Index
Study Overview
Status
Intervention / Treatment
Detailed Description
Peripheral nerve block is to anesthetize the dermatomes belonging to the nerve or nerve group to which the block is applied, by performing sympathetic, sensory and motor blocks. Brachial plexus blockade; It is a peripheral nerve blockage that can be used in surgical operations to be performed on the upper extremity and can be performed at the level of interscalene, supraclavicular, infraclavicular, costoclavicular, axillary and terminal nerves.
The costoclavicular brachial plexus block has been used as an alternative to lateral sagittal infraclavicular block, due to its ease of application, its rapid onset of action and its high success rate. The effectiveness of the block is measured by sensory, motor and sympathetic block effects. The sensory block can be evaluated by cold or pinprick test, and motor block by traditional methods such as the patient's response to verbal commands and can be objective.
Sympathetic block manifests itself with vasodilation and an increase in blood flow rate and can be measured with the more quantitative perfusion index (PI). The perfusion index represents the ratio of pulsatile blood flow to static blood flow in peripheral tissue and can be measured continuously and noninvasively from a pulse oximeter. Successful peripheral nerve blockade; It is seen as local vasodilation, increased local blood flow, some increase in skin temperature and loss of sensation in the extremity due to the blockage of sympathetic fibers. It can be a guide in determining the effectiveness of the block because it is noninvasive and easy, providing rapid evaluation, without requiring patient cooperation to evaluate the success of the block.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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İzmir, Turkey, 35360
- Katip Çelebi University İzmir Atatürk Training and Reseach Hospital
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İzmir, Turkey, 35360
- Katip Celebi University Ataturk Training and Research Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All costoclavicular and infraclavicular block patients who have undergone hand,forearm and arm surgery
- Patients over the age of 18
Exclusion Criteria:
- Patients who do not want to participate in the study
- Patients whose peripheral block administration is contraindicated
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Infraclavicular Group
Block Characteristics of Ultrasound Guided Infraclavicular Block with the Perfusion Index
|
perfusion index in the prediction of peripheral block success was previously reported for infraclavicular brachial plexus block, axillary brachial plexus block, interscalene brachial plexus block, and supraclavicular brachial plexus in adult patients
|
|
Costoclavicular Group
Block Characteristics of Ultrasound Guided costoclavicular Block with the Perfusion Index
|
perfusion index in the prediction of peripheral block success was previously reported for infraclavicular brachial plexus block, axillary brachial plexus block, interscalene brachial plexus block, and supraclavicular brachial plexus in adult patients
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation of perfusion index with infraclavicular and costoclavicular block success
Time Frame: 3 Months
|
Correlation of perfusion index with infraclavicular and costoclavicular block success
|
3 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison of the Block Characteristics of Ultrasound Guided Costoclavicular and Infraclavicular Block
Time Frame: 3 Months
|
Comparison of the Block Characteristics of Ultrasound Guided Costoclavicular and Infraclavicular Block
|
3 Months
|
Collaborators and Investigators
Investigators
- Study Director: Busra Serce, MD, KCU Izmir Atatürk Training and Research Hospital
- Principal Investigator: Derya Yurtlu, MD, KCU Izmir Atatürk Training and Research Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IATRH
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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