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Time-differentiated Therapeutic Hypothermia (TTH48)

Primary Purpose

Out of Hospital Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Therapeutic hypothermia
Sponsored by
University of Aarhus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Out of Hospital Cardiac Arrest

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Out of hospital cardiac arrest of suspected cardiac origin
  2. Return of spontaneous circulation (ROSC)
  3. Glasgow Coma Score < 8
  4. Estimated time interval from cardiac arrest to ROSC ≤ 60 min

Exclusion Criteria:

  1. OOH-CA of suspected origin other than cardiac
  2. In hospital Cardiac arrest
  3. Terminal disease
  4. Coagulation disorders
  5. Unwitnessed asystolia
  6. Time from cardiac arrest to start of hypothermia treatment > 240 min
  7. GCS ≥ 8
  8. Pregnancy
  9. Persistent cardiogenic shock (Systolic blood pressure < 80 mmHg despite inotropic treatment and aortic balloon pump).
  10. CPC 3-4 before cardiac arrest
  11. Acute intra cerebral bleeding
  12. Acute stroke
  13. Acute coronary artery bypass grafting

Sites / Locations

  • Department of Intensive Care, Erasme Hospital
  • Department of Anesthesiology and Intensive Care Medicine, Aarhus University Hospital, Aalborg
  • Department og Anesthesiologi and Intensive Care Medicine,
  • Department of Cardiology, Copenhagen University Hospital, Rigshospitalet
  • Department of Anaesthesiology and Intensive Care Medicine, Odense University Hospital
  • Anaesthesiology Clinic, North Estonia Medical Centre
  • Division of Anaesthesiology and Intensive Care Medicine, Department of Surgery, Helsinki University Central Hospital
  • Hospital District of Southwest Finland), Kiinamyllynkatu
  • Department of Internal Medicine, Nephrology and Intensive Care; Charité-Universitätsmedizin Berlin
  • Anesthesiology and Critical Care, Stavanger University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

24 hours hypothermia

48 hours hypothermoa

Arm Description

24 hours hypothermia

48 hours hypothermia

Outcomes

Primary Outcome Measures

CPC
CPC = Cerebral Performance Category Score. The primary outcome of the study is analyzed as the proportion of patients with good neurological outcome in the two groups, (CPC 1-2) at 6 months after CA.

Secondary Outcome Measures

Adverse events
Adverse events are registered during the treatment and until discharge from primary hospital unit
CPC at discharge
CPC at discharge from primary hospital unit and after 28 days plus after 3 month
Mortality
CPC 5 at 6 month

Full Information

First Posted
September 17, 2012
Last Updated
January 17, 2017
Sponsor
University of Aarhus
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1. Study Identification

Unique Protocol Identification Number
NCT01689077
Brief Title
Time-differentiated Therapeutic Hypothermia
Acronym
TTH48
Official Title
Time-differentiated Treatment With Mild Therapeutic Hypothermia Following Cardiac Arrest, a Multi Center Study.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
January 2017 (Actual)
Study Completion Date
January 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if 48 hours of mild therapeutic hypothermia following out of hospital cardiac arrest gives a better cerebral outcome compared to 24 hours therapeutic hypothermia.
Detailed Description
Sudden out-of-hospital cardiac arrest (OOH-CA) remains a significant cause of death. However, in 2002 it was in two clinical trials demonstrated that mild therapeutic hypothermia in comatose OOH-CA victims yields a better cerebral outcome measured by Cerebral Performance Category Score (CPC) after 6 month. The optimal mild hypothermia treatment time is however not known. The two trials from 2002 apply the treatment for 12 and 24 hours respectively. In newborns with cerebral hypoxic damage the standard treatment time is 72 hours. It is therefore relevant to investigate the influence of the treatment time on the cerebral outcome in OOH-CA victims. In the present study cerebral outcome after mild therapeutic hypothermia (target temperature 33 degrees centigrade) in OOH-CA patients for 24 is compared to outcome after 48 hours of mild hypothermia. The main outcome parameter is mortality and CPC score measured 6 month after the treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Out of Hospital Cardiac Arrest

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
355 (Actual)

8. Arms, Groups, and Interventions

Arm Title
24 hours hypothermia
Arm Type
Active Comparator
Arm Description
24 hours hypothermia
Arm Title
48 hours hypothermoa
Arm Type
Experimental
Arm Description
48 hours hypothermia
Intervention Type
Other
Intervention Name(s)
Therapeutic hypothermia
Intervention Description
Mild therapeutic hypothermia with a target temperature of 33 degrees Centigrade for 24 or 48 hours
Primary Outcome Measure Information:
Title
CPC
Description
CPC = Cerebral Performance Category Score. The primary outcome of the study is analyzed as the proportion of patients with good neurological outcome in the two groups, (CPC 1-2) at 6 months after CA.
Time Frame
6 month
Secondary Outcome Measure Information:
Title
Adverse events
Description
Adverse events are registered during the treatment and until discharge from primary hospital unit
Time Frame
10 days
Title
CPC at discharge
Description
CPC at discharge from primary hospital unit and after 28 days plus after 3 month
Time Frame
3 month
Title
Mortality
Description
CPC 5 at 6 month
Time Frame
6 month
Other Pre-specified Outcome Measures:
Title
GCS
Description
Glasgow Coma Score at day 4 and at discharge from primary hospital unit
Time Frame
28 days
Title
GCS progression
Description
Glasgow Coma Score throughout the observation period
Time Frame
25 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Out of hospital cardiac arrest of suspected cardiac origin Return of spontaneous circulation (ROSC) Glasgow Coma Score < 8 Estimated time interval from cardiac arrest to ROSC ≤ 60 min Exclusion Criteria: OOH-CA of suspected origin other than cardiac In hospital Cardiac arrest Terminal disease Coagulation disorders Unwitnessed asystolia Time from cardiac arrest to start of hypothermia treatment > 240 min GCS ≥ 8 Pregnancy Persistent cardiogenic shock (Systolic blood pressure < 80 mmHg despite inotropic treatment and aortic balloon pump). CPC 3-4 before cardiac arrest Acute intra cerebral bleeding Acute stroke Acute coronary artery bypass grafting
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans Kirkegaard, Professor
Organizational Affiliation
Department of Anaesthesia and Intensive care medicine, Aarhus University Hosptal, Brendstrupgaardsvej 8200 Aarhus, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Intensive Care, Erasme Hospital
City
Brussels
ZIP/Postal Code
1070
Country
Belgium
Facility Name
Department of Anesthesiology and Intensive Care Medicine, Aarhus University Hospital, Aalborg
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark
Facility Name
Department og Anesthesiologi and Intensive Care Medicine,
City
Aarhus
ZIP/Postal Code
8200
Country
Denmark
Facility Name
Department of Cardiology, Copenhagen University Hospital, Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark
Facility Name
Department of Anaesthesiology and Intensive Care Medicine, Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Facility Name
Anaesthesiology Clinic, North Estonia Medical Centre
City
Tallinn
ZIP/Postal Code
13419
Country
Estonia
Facility Name
Division of Anaesthesiology and Intensive Care Medicine, Department of Surgery, Helsinki University Central Hospital
City
Helsinki
ZIP/Postal Code
00029-HUS
Country
Finland
Facility Name
Hospital District of Southwest Finland), Kiinamyllynkatu
City
Turku
Country
Finland
Facility Name
Department of Internal Medicine, Nephrology and Intensive Care; Charité-Universitätsmedizin Berlin
City
Berlin
Country
Germany
Facility Name
Anesthesiology and Critical Care, Stavanger University Hospital
City
Stavanger
ZIP/Postal Code
4068
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
35907787
Citation
Larsen AI, Grejs AM, Vistisen ST, Strand K, Skadberg O, Jeppesen AN, Duez CHV, Kirkegaard H, Soreide E. Kinetics of 2 different high-sensitive troponins during targeted temperature management in out-of-hospital cardiac arrest patients with acute myocardial infarction: a post hoc sub-study of a randomised clinical trial. BMC Cardiovasc Disord. 2022 Jul 30;22(1):342. doi: 10.1186/s12872-022-02778-4.
Results Reference
derived
PubMed Identifier
34375135
Citation
Bach HM, Duez CHV, Jeppesen AN, Strand K, Soreide E, Kirkegaard H, Grejs AM. MR-proANP and NT-proBNP During Targeted Temperature Management Following Out-of-Hospital Cardiac Arrest: A Post hoc Analysis of the TTH48 Trial. Ther Hypothermia Temp Manag. 2022 Jun;12(2):82-89. doi: 10.1089/ther.2021.0012. Epub 2021 Aug 10.
Results Reference
derived
PubMed Identifier
33181415
Citation
Hastbacka J, Kirkegaard H, Soreide E, Taccone FS, Rasmussen BS, Storm C, Kjaergaard J, Laitio T, Duez CHV, Jeppesen AN, Grejs AM, Skrifvars MB. Severe or critical hypotension during post cardiac arrest care is associated with factors available on admission - a post hoc analysis of the TTH48 trial. J Crit Care. 2021 Feb;61:186-190. doi: 10.1016/j.jcrc.2020.10.026. Epub 2020 Nov 2.
Results Reference
derived
PubMed Identifier
31830304
Citation
Skrifvars MB, Soreide E, Sawyer KN, Taccone FS, Toome V, Storm C, Jeppesen A, Grejs A, Duez CHV, Tiainen M, Rasmussen BS, Laitio T, Hassager C, Kirkegaard H. Hypothermic to ischemic ratio and mortality in post-cardiac arrest patients. Acta Anaesthesiol Scand. 2020 Apr;64(4):546-555. doi: 10.1111/aas.13528. Epub 2019 Dec 26.
Results Reference
derived
PubMed Identifier
30572070
Citation
Evald L, Bronnick K, Duez CHV, Grejs AM, Jeppesen AN, Soreide E, Kirkegaard H, Nielsen JF. Prolonged targeted temperature management reduces memory retrieval deficits six months post-cardiac arrest: A randomised controlled trial. Resuscitation. 2019 Jan;134:1-9. doi: 10.1016/j.resuscitation.2018.12.002. Epub 2018 Dec 17.
Results Reference
derived
PubMed Identifier
28742911
Citation
Kirkegaard H, Soreide E, de Haas I, Pettila V, Taccone FS, Arus U, Storm C, Hassager C, Nielsen JF, Sorensen CA, Ilkjaer S, Jeppesen AN, Grejs AM, Duez CHV, Hjort J, Larsen AI, Toome V, Tiainen M, Hastbacka J, Laitio T, Skrifvars MB. Targeted Temperature Management for 48 vs 24 Hours and Neurologic Outcome After Out-of-Hospital Cardiac Arrest: A Randomized Clinical Trial. JAMA. 2017 Jul 25;318(4):341-350. doi: 10.1001/jama.2017.8978.
Results Reference
derived
PubMed Identifier
27894327
Citation
Kirkegaard H, Pedersen AR, Pettila V, Hjort J, Rasmussen BS, de Haas I, Nielsen JF, Ilkjaer S, Kaltoft A, Jeppesen AN, Grejs AM, Duez CH, Larsen AI, Toome V, Arus U, Taccone FS, Storm C, Laitio T, Skrifvars MB, Soreide E. A statistical analysis protocol for the time-differentiated target temperature management after out-of-hospital cardiac arrest (TTH48) clinical trial. Scand J Trauma Resusc Emerg Med. 2016 Nov 28;24(1):138. doi: 10.1186/s13049-016-0334-0.
Results Reference
derived
PubMed Identifier
27142588
Citation
Kirkegaard H, Rasmussen BS, de Haas I, Nielsen JF, Ilkjaer S, Kaltoft A, Jeppesen AN, Grejs A, Duez CH, Larsen AI, Pettila V, Toome V, Arus U, Taccone FS, Storm C, Skrifvars MB, Soreide E. Time-differentiated target temperature management after out-of-hospital cardiac arrest: a multicentre, randomised, parallel-group, assessor-blinded clinical trial (the TTH48 trial): study protocol for a randomised controlled trial. Trials. 2016 May 4;17(1):228. doi: 10.1186/s13063-016-1338-9.
Results Reference
derived

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Time-differentiated Therapeutic Hypothermia

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