Dynamics of the Capillary Lactate Levels in OHCA

January 17, 2022 updated by: Matej Strnad, University Medical Centre Maribor

Dynamics of the Capillary Lactate Levels in Patients With Out-of-hospital Cardiac Arrest

Serial capillary lactate measurements during cardiopulmonary resuscitation (CPR) in patients with out-of-hospital cardiac arrest (OHCA).

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Capillary lactate measurements will be measured every ten minutes during CPR in OHCA.

Study Type

Observational

Enrollment (Anticipated)

100

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Vitka Vujanović, MD
  • Phone Number: + 386 41 927 555
  • Email: vitkav@gmail.com

Study Locations

  • Slovenia
      • Maribor, Slovenia, 2000
        • Recruiting
        • Community health center Maribor, Prehospital unit
        • Contact:

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

For this study will be eligible all patients with OHCA due to primary or secondary cardiac arrest.

Description

Inclusion Criteria:

  • adults with OHCA

Exclusion Criteria:

  • children with OHCA
  • trauma
  • hypothermia

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

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ROSC
Time Frame: 2 years
In patients with ROSC the capillary lactate level will be lower compare to the non ROSC group.
2 years
Comparison between primary and secondary cardiac arrest
Time Frame: 2 years
Initial and serial values of capillary lactate will be lower in patients with primary out-of- hospital cardiac arrest (OHCA)
2 years
No ROSC
Time Frame: 2 years
Serial values of capillary lactate will be higher in patients without ROSC
2 years

Collaborators and Investigators

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

Sponsor

University Medical Centre Maribor

Investigators

  • Study Director: Matej Strnad, MD, PhD, University medical center Maribor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

April 1, 2019

Primary Completion (Actual)

December 31, 2021

Study Completion (Anticipated)

May 31, 2022

Study Registration Dates

First Submitted

September 24, 2020

First Submitted That Met QC Criteria

September 24, 2020

First Posted (Actual)

October 1, 2020

Study Record Updates

Last Update Posted (Actual)

January 19, 2022

Last Update Submitted That Met QC Criteria

January 17, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KME 0120-229/2018/12

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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