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

• Sponsor: Tokat Gaziosmanpasa University (Other)
• Overall Status: Completed
• CT.gov ID: NCT02727829
• Collaborator: (none)
• Enrollment: 50
• Actual Duration (Months): 5

Study Details

Study Description

Brief Summary

The aim of the present study is to assess the effects of brachial plexus block on microcirculation using pefusion index and capillary filling time.

Condition or Disease	Intervention/Treatment	Phase
Circulatory; Change	Device: pefusion index measurement

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 Design

• Study Type: Observational
• Actual Enrollment: 50 participants
• Observational Model: Other
• Time Perspective: Prospective
• Official Title: The Assessment of Microcirculation in Brachial Plexus Block Using Perfusion Index and Capillary Filling Time
• Actual Study Start Date: May 1, 2016
• Actual Primary Completion Date: Oct 1, 2016
• Actual Study Completion Date: Oct 1, 2016

Outcome Measures

Primary Outcome Measures

1. perfusion index [five times in one year]

Secondary Outcome Measures

1. capillary filing time [five times in one year]

2. heart rate [five times in one year]

3. blood pressure [five times in one year]

4. oxygen saturation [five times in one year]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 70 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

• Tokat Gaziosmanpasa University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: humeyra astan, Resident, Tokat Gaziosmanpasa University
• ClinicalTrials.gov Identifier: NCT02727829
• Other Study ID Numbers: 15-KAEK-221
• First Posted: Apr 5, 2016
• Last Update Posted: Feb 14, 2017
• Last Verified: Feb 1, 2017

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No

Study Results

No Results Posted as of Feb 14, 2017