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Completed

NCT Number: NCT04857216

Comparison of the Block Characteristics of USG Guided Costoclavicular and Infraclavicular Block With the Perfusion Index

With this study, it was aimed to compare the block characteristics evaluated with traditional methods in infraclavicular and costoclavicular block applications performed in upper extremity surgery in our clinic with the perfusion index

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Katip Celebi University Atatürk Training and Research Hospital, Izmir, Turkey (Türkiye)

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About this study

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.

Who can participate

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

perfusion index

Device

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

Primary outcomes

  1. Correlation of perfusion index with infraclavicular and costoclavicular block success

    Time frame: 3 Months

    Correlation of perfusion index with infraclavicular and costoclavicular block success

Secondary outcomes

  1. 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

Sponsors and collaborators

Lead sponsor

Izmir Ataturk Training and Research Hospital

Other

Registry information

Official study title

Comparison of the Block Characteristics of Ultrasound Guided Costoclavicular and Infraclavicular Block With the Perfusion Index

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Apr 23, 2021
Registry last updated
Sep 1, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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