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Goal-directed CPR Using Cerebral Oximetry

NYU Langone Health logo

NYU Langone Health

Status

Active, not recruiting

Conditions

Ischemia
Reperfusion Injury

Treatments

Other: Non-Physiological Feedback CPR
Other: Physiological Feedback CPR

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04924985
20-00354
1R01HL151732-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The proposed study is a single-center, randomized controlled pilot trial of adults who suffer in-hospital cardiac arrests. Using cerebral oxygenation and end-tidal carbon dioxide physiological targets to predict survival and neurological outcome, the impact of physiological-feedback CPR will be assessed. 150 adult patients who have a cardiac arrest event at NYU Tisch Hospital will be randomized to one of two treatment groups: (1) Physiological-Feedback CPR or (2) Non-Physiological (Audiovisual) Feedback CPR.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. In-hospital cardiac arrest patient
  2. Age ≥18 years
  3. Age <80 years
  4. CPR lasting ≥5 minutes

Exclusion criteria

  1. Patients < 18 years of age or > 80 years of age
  2. Out of hospital cardiac arrest patients
  3. ≥3 acute organ failures (defined as acute renal failure requiring dialysis, fulminant liver failure i.e. liver failure with INR≥1.5, respiratory failure requiring mechanical ventilation)
  4. Repeat in-hospital cardiac arrest event within 14 days of a prior cardiac arrest
  5. Presence of known raised intracranial pressure
  6. Presence of known traumatic brain injury or subarachnoid hemorrhage <14 days old, frontal lobe brain tumors or subdural hemorrhage
  7. Hyperbilirubinemia >1.0 mg/dl (based on the absorption of near-infrared light by bilirubin)
  8. Resuscitation using extra-corporeal membrane oxygenation (ECMO)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups

Physiological Feedback CPR
Experimental group
Treatment:
Other: Physiological Feedback CPR
Non-Physiological (Audiovisual) Feedback CPR
Active Comparator group
Treatment:
Other: Non-Physiological Feedback CPR

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Anelly Gonzalez; Natalia Leontovich

Data sourced from clinicaltrials.gov

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