Study Stopped
Not feasible
Arterial Blood Pressure and Cardiac Arrest
ABaCAS
1 other identifier
observational
N/A
0 countries
N/A
Brief Summary
To describe and measure diastolic and systolic femoral arterial pressure during medical cardiac arrest. To define baseline measures. To describe and measure arterial blood pressure after placement of an ITD device. To observe the diastolic pressure immediately prior to return of spontaneous circulation. To quantify and describe the effects of intravenous adrenaline on arterial blood pressure in cardiac arrest.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Sep 2024
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 30, 2024
CompletedFirst Posted
Study publicly available on registry
June 5, 2024
CompletedStudy Start
First participant enrolled
September 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2025
CompletedSeptember 25, 2025
September 1, 2025
3 months
May 30, 2024
September 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
systolic femoral invasive blood pressure
3 mins average with CPR by LUCAS device
Secondary Outcomes (2)
femoral diastolic pressure
3 mins average with CPR by LUCAS device
femoral arterial pressure, both systolic and diastolic
3 mins average post placement of ICD device
Study Arms (1)
adult cardiac arrest
blood pressure measurement pre and post impedance threshold device placement
Interventions
impedance threshold device (ResQPOD, Zoll) applied to airway
Eligibility Criteria
Adult patients (18+) suffering an out of hospital cardiac arrest (OHCA) by a presumed medical cause that have been deemed suitable to attempt resuscitation of. All individuals will be considered for inclusion in this study regardless of age, disability, gender reassignment, marriage, and civil partnership, pregnancy and maternity, race, religion and belief, sex, and sexual orientation except where the study inclusion and exclusion criteria EXPLICITLY state otherwise.
You may qualify if:
- Adult patients (≥18years) in medical cardiac arrest
- Deemed suitable to attempt resuscitation.
You may not qualify if:
- Prisoners
- \<18years
- Pregnancy
- Traumatic cardiac arrest
- Arrest caused by hypovolaemia, tension or tamponade as determined by the clinical team on scene
- Inability to secure a patent airway.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 30, 2024
First Posted
June 5, 2024
Study Start
September 1, 2024
Primary Completion
December 1, 2024
Study Completion
June 1, 2025
Last Updated
September 25, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share