Prospective Investigation of Antithrombin III Deficiency in Adult Patients With ECMO

Sponsor
Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04879550
Collaborator
(none)
50
1
26
1.9

Study Details

Study Description

Brief Summary

There are publications showing a decrease in Antithrombin III levels of continuous flow and routine heparin therapy in adult patients undergoing Extracorporeal Membrane Oxygenation (ECMO) however, there is not enough data. One of the multifactorial causes affecting bleeding / thrombosis complications and ACT levels may be acquired Antithrombin III deficiency.

The Antithrombin III activity test results from the patients to be included in the study during the study will be recorded immediately after ECMO run, at the 24th hour before the heparin infusion start and at the 48th, 72nd and 96th hours following the follow-up. The results will be analyzed to figure out a relationship between decreasing Antithrombin 3 values and thrombotic events.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Antithrombin III

Detailed Description

ECMO is applied in patients with acute severe heart or lung failure. The treatment protocol of patients undergoing ECMO is carefully arranged against the risk of bleeding / thrombosis.

According to the general protocol, heparin infusion therapy is started at the 24th hour after ECMO application. The risk of bleeding / thrombosis is avoided by adjusting the heparin infusion dose with Activated Clotting Time (ACT) control. However, over time, thrombocytopenia and fluctuations in ACT level are observed in patients. It may be necessary to increase the dose of heparin given during the prolonged period. One of the multifactorial causes affecting bleeding / thrombosis complications and ACT levels may be acquired Antithrombin III deficiency. There are publications reporting a decrease in Antithrombin III levels of continuous flow and routine heparin therapy in adult patients undergoing ECMO; however, there is not enough data.

The Antithrombin III activity test results from the patients to be included in the study during the study will be recorded immediately after ECMO run, at the 24th hour before the heparin infusion start and at the 48th, 72nd and 96th hours following the follow-up. The results will be analyzed to figure out a relationship between decreasing Antithrombin 3 values and thrombotic events.

Study Design

Study Type:
Observational
Actual Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Investigation of the Association of Antithrombin III Deficiency With Thrombotic Events in Adult Patients With ECMO
Actual Study Start Date :
Jan 1, 2020
Actual Primary Completion Date :
Jan 1, 2022
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
thrombotic event developing / not

Group I: Patients with no bleeding/thrombosis complications Group II: Patients with Thrombotic and/or thromboembolic complications Group III: Patients with bleeding complications

Diagnostic Test: Antithrombin III
Antithrombin III deficiency causes thrombosis. Is thrombosis in ECMO patients related to Antithrombin III deficiency? Groups with and without thrombosis will be separated and whether it is related to Antithrombin III deficiency will be evaluated.

Outcome Measures

Primary Outcome Measures

  1. Antithrombin 3 activity level [5 days]

    Antithrombin 3 activity test levels will be checked in the first 5 days after ecmo application.

Secondary Outcome Measures

  1. Thrombosis and Bleeding Events [1 week]

    Thrombotic or bleeding complications occurring during ECMO run

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being over the age of 18

  • Patients with ECMO run for 3 days or more (to be able to determine at least 3 antithrombin 3 levels)

Exclusion Criteria:
  • Patients with ECMO run less than 3 days

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul Dr.Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital Istanbul Turkey 34668

Sponsors and Collaborators

  • Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

Investigators

  • Study Director: Serap AKA, Cardiovascular Surgeon

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Arif Yasin Çakmak, Principal Investigator, Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital
ClinicalTrials.gov Identifier:
NCT04879550
Other Study ID Numbers:
  • HNEAH-KAEK 2019/81-866
First Posted:
May 10, 2021
Last Update Posted:
May 24, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Arif Yasin Çakmak, Principal Investigator, Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2022