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

NCT04857216 | Completed

• 1 other identifier: IATRH
• Study Type: observational
• Target: 90
• Locations: 1 country
• Sites: 2

Brief Summary

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

Conditions

Costoclavicular and Infraclavicular Block for Patients Who Have Undergone Hand,Forearm and Arm Surgery

Keywords

infraclavicular, costoclavicular, perfusion index, block

Outcome Measures

Primary Outcomes (1)

• Correlation of perfusion index with infraclavicular and costoclavicular block success

  Correlation of perfusion index with infraclavicular and costoclavicular block success

  3 Months

Secondary Outcomes (1)

• Comparison of the Block Characteristics of Ultrasound Guided Costoclavicular and Infraclavicular Block

  3 Months

Study Arms (2)

Infraclavicular Group

Block Characteristics of Ultrasound Guided Infraclavicular Block with the Perfusion Index

Device: Perfusion Index

Costoclavicular Group

Block Characteristics of Ultrasound Guided costoclavicular Block with the Perfusion Index

Device: Perfusion Index

Interventions

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

Costoclavicular Group; Infraclavicular Group

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Probability Sample

Study Population

All costoclavicular and infraclavicular block patients who have undergone hand,forearm and arm surgery over the age of 18

You may qualify if:

• All costoclavicular and infraclavicular block patients who have undergone hand,forearm and arm surgery
• Patients over the age of 18

You may not qualify if:

• Patients who do not want to participate in the study
• Patients whose peripheral block administration is contraindicated

Sponsors & Collaborators

• Izmir Ataturk Training and Research Hospital: lead

Study Sites (2)

Katip Celebi University Atatürk Training and Research Hospital

Izmir, 35360, Turkey (Türkiye)

Location

Katip Çelebi University İzmir Atatürk Training and Reseach Hospital

Izmir, 35360, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Bites and Stings

Interventions

Perfusion Index

Condition Hierarchy (Ancestors)

Poisoning; Chemically-Induced Disorders; Wounds and Injuries

Intervention Hierarchy (Ancestors)

Diagnostic Techniques, Cardiovascular; Diagnostic Techniques and Procedures; Diagnosis

Study Officials

• Busra Serce, MD

  KCU Izmir Atatürk Training And Research Hospital

  STUDY DIRECTOR

• Derya Yurtlu, MD

  KCU Izmir Atatürk Training And Research Hospital

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Target Duration: 3 Months
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Associate Professor

Study Record Dates

• First Submitted: April 21, 2021
• First Posted: April 23, 2021
• Study Start: March 14, 2021
• Primary Completion: June 30, 2021
• Study Completion: July 30, 2021
• Last Updated: September 1, 2021

Record last verified: 2021-08

Locations

TU (2)