The Assessment of Microcirculation in Brachial Plexus Block Using Perfusion Index and Capillary Filling Time

February 13, 2017 updated by: humeyra astan, Tokat Gaziosmanpasa University
The aim of the present study is to assess the effects of brachial plexus block on microcirculation using pefusion index and capillary filling time.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Microcirculation is very crucial to evaluate the organ function those working properly in human body. The aim of the present study is to assess the effects of brachial plexus block on microcirculation using pefusion index and capillary filling time. A total of 50 patients whose planned to underwent surgery are performed brachial plexus block using ultrasound, and pefusion index, heart rate, blood pressure, capillary filling time are measured at 0, 10th and 20th minutes interval and at postoperative 24th hours. All measures will be recorded.

Study Type

Observational

Enrollment (Actual)

50

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

  • American Society of Anesthesiologists score of I and III
  • ages between 18 and 70
  • upper extremity surgery

Description

Inclusion Criteria:

  • American Society of Anesthesiologists score of I and III
  • ages between 18 and 70
  • upper extremity surgery

Exclusion Criteria:

  • not to participate in the study
  • reject to perform the intervention
  • infection in injection cite
  • allergy to local anesthetics
  • peripherical vasculary diseases
  • psychiatric diseases
  • coagulation anomalies

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
perfusion index
Time Frame: five times in one year
five times in one year

Secondary Outcome Measures

Outcome Measure
Time Frame
capillary filing time
Time Frame: five times in one year
five times in one year
heart rate
Time Frame: five times in one year
five times in one year
blood pressure
Time Frame: five times in one year
five times in one year
oxygen saturation
Time Frame: five times in one year
five times in one year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Tokat Gaziosmanpasa University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2016

Primary Completion (Actual)

October 1, 2016

Study Completion (Actual)

October 1, 2016

Study Registration Dates

First Submitted

March 30, 2016

First Submitted That Met QC Criteria

March 30, 2016

First Posted (Estimate)

April 5, 2016

Study Record Updates

Last Update Posted (Actual)

February 14, 2017

Last Update Submitted That Met QC Criteria

February 13, 2017

Last Verified

February 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 15-KAEK-221

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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