ISRCTN ISRCTN82347313
DOI https://doi.org/10.1186/ISRCTN82347313
ClinicalTrials.gov number NCT00219687
Secondary identifying numbers N0352143844
Submission date
29/09/2006
Registration date
29/09/2006
Last edited
12/04/2012
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Circulatory System
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English Summary

Not provided at time of registration

Contact information

Dr Rachael T Donohoe
Scientific

London Ambulance Service NHS Trust - Headquarters Annexe
Ground Floor
8-20 Pocock Street
London
SE1 0BW
United Kingdom

Phone +44 020 7463 3126
Email rachael.donohoe@lond-amb.nhs.uk

Study information

Study designRandomised controlled trial
Primary study designInterventional
Secondary study designRandomised controlled trial
Study setting(s)Not specified
Study typeTreatment
Participant information sheet No information is supplied to patients as they are in cardiac arrest when enrolled in the study. The protocol is fully approved by a Research Ethics Committee and is compliant with relevant legislation relating to trials in emergency situations.
Scientific titleDispatcher-Assisted Resuscitation Trial
Study acronymDART
Study hypothesisIs telephone-assisted CPR with chest compressions only better than telephone-assisted CPR with ventilation and compressions? Which protocol will save more lives?
Ethics approval(s)Added 24 July 2008:
Approved by Lewisham Research Ethics Committee (UK) on 04/08/2004. Reference 04/Q0701/07.
ConditionCardiovascular: Cardiac arrest
InterventionDispatcher-assisted CPR instructions with compressions and ventilations versus dispatcher-assisted CPR instructions with compressions only
Intervention typeOther
Primary outcome measureSurvival to hospital discharge
Secondary outcome measuresAdded 24 July 2008:
Neurological status at hospital discharge (United States only).
Overall study start date01/06/2004
Overall study end date30/09/2008

Eligibility

Participant type(s)Patient
Age groupAdult
SexBoth
Target number of participantsThe total sample size for the study is approximately 1600 patients.
Participant inclusion criteriaAll cardiac arrest patients for whom the LAS is contacted, who are not breathing or conscious, and the caller is amenable to undertaking dispatcher-assisted CPR.
Participant exclusion criteria1. Caller refusal to undertake CPR
2. CPR already in progress
3. Cases of cardiac arrest due to trauma, electrocution, hanging, drowning or strangulation
4. AED available for use
5. Vulnerable groups: <18 years, pregnant women, prisoners (if data is known)
Recruitment start date01/06/2004
Recruitment end date30/09/2008

Locations

Countries of recruitment

  • England
  • United Kingdom
  • United States of America

Study participating centre

London Ambulance Service NHS Trust - Headquarters Annexe
London
SE1 0BW
United Kingdom

Sponsor information

Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Government

The Department of Health, Richmond House, 79 Whitehall
London
SW1A 2NL
United Kingdom

Phone +44 (0)20 7307 2622
Email dhmail@doh.gsi.org.uk
Website http://www.dh.gov.uk/Home/fs/en

Funders

Funder type

Government

London Ambulance Service NHS Trust (UK)

No information available

NHS R&D Support Funding

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article results 29/07/2010 Yes No