Measurement of Cut-off Perfusion Index Value in Infraclavicular Blocks

Upper Extremity Surgery Clinical Trial

Official title:

To Investigate the Value of the Cut-off Perfusion Index Showing That the Block is Successful in Infraclavicular Blocks Performed Under Ultrasound Guidance.

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT05234541
• Other study ID #: 2020/6-18
• Secondary ID: ISEYHANLI
• Status: Active, not recruiting
• Start date: July 1, 2021
• Est. completion date: November 15, 2022

Study information

• Verified date: July 2021
• Source: Adiyaman University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

To investigate the value of the cut-off perfusion index showing that the block is successful in infraclavicular blocks performed under ultrasound guidance.

Description:

In upper extremity procedures, ultrasound (US) guided infraclavicular block is a frequently used approach. Today, the frequency of studies on the perfusion index (PI), which can be used as a criterion in the evaluation of block success, is increasing. The aim of this study is to evaluate the success and effectiveness of infraclavicular approach block with perfusion index using ROC (Receiver Operating Characteristic) curves.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 1
• Est. completion date: November 15, 2022
• Est. primary completion date: April 15, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• ASA 1-2 PATIENTS

• PATIENTS BETWEEN 18-65 YEARS

• PATIENTS WITH INFRACLAVICULAR BLOCK

Exclusion Criteria:

• ASA3-4 PATIENTS

• PATIENTS UNDER THE AGE OF 18, PATIENTS OVER 65

• PATIENTS WHO DO NOT WANT TO BE INCLUDED IN THE STUDY

• PATIENTS WITH CONTRAINDICATION TO INFRACLAVICULAR BLOCK

• PATIENTS WITHOUT COOPERATION

• PATIENTS WITH DIABETES MELLITUS

• THOSE WHO HAVE PERIPHERAL ARTERY DISEASE

Related Conditions & MeSH terms

• Upper Extremity Surgery

Locations

Country	Name	City	State
Turkey	Adiyaman University Recruitment	Adiyaman

Sponsors (1)

Lead Sponsor	Collaborator
Adiyaman University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To Investigate the Value of the Cut-off Perfusion Index Showing That the Block is Successful in Infraclavicular Blocks Performed Under Ultrasound Guidance	To measure perfusion index values in patients aged 18-65 years who underwent upper extremity surgery	Perfusion index, pulse and blood pressure will be measured 5-10-20 minutes after the block is made.