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Active, not recruiting Not applicable

Effect of Electrically Insulated Gloves on ROSC Time, End-tidal CO₂ Response, Survival and Morbidity in Uninterrupted CPR

NCT07299188 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-11-06
Last updated
2025-12-30

Condition(s) studied

Cardiopulmonary Resuscitation (CPR)Electrical ShockDefibrillation

Investigational drug(s) / intervention(s)

HANDS ON BUT OFF DEFIBRILLATION

HANDS ON BUT OFF DEFIBRILLATION: GROUP WHICH LL BE APPLIED STANDARD CPR PROTOCOL OF AHA BY USING ELECTRICALLY ISOLATED GLOVES

Study summary

Cardiopulmonary arrest is the sudden cessation of spontaneous breathing and circulation due to various causes. Cardiopulmonary resuscitation (CPR) is the set of decisions and procedures encompassing all efforts aimed at restoring spontaneous circulation. Guidelines are published at regular intervals by the American Heart Association (AHA) and the European Resuscitation Council (ERC) to ensure that these procedures are applied uniformly worldwide. According to the AHA and ERC guidelines, the latest approach to CPR is to reduce the duration of interruptions in chest compressions, which is a component of high-quality CPR. Prior to actual patient intervention, a preliminary test will be conducted on an advanced life support simulation manikin to evaluate the safety and feasibility of the method.

During cardiopulmonary resuscitation (CPR), unavoidable interruptions in chest compressions occur because contact with the patient must be broken during defibrillation and cardioversion. In this study, electrically insulated composite gloves (Class 2) will be used to ensure uninterrupted chest compressions during defibrillation, and the effect of this practice on patients' ROSC, EtCO₂, neurological outcomes, and survival rates will be evaluated comparatively with the control group.

The main objective of the study is to evaluate the effect of ensuring uninterrupted chest compressions during defibrillation using electrically insulated composite gloves on patient survival rates.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients diagnosed with in-hospital cardiac arrest requiring CPR * Patients with shockable rhythms (pulseless ventricular tachycardia (VT) and ventricular fibrillation (VF)) * Adult patients aged 18 years and older * Patients capable of providing informed consent or for whom consent can be obtained through a legal representative Exclusion Criteria: * Out-of-hospital cardiac arrests * Patients who received CPR outside the emergency department * Traumatic patients * Pregnant patients * Patients under 18 years of age * Terminally ill patients

Primary outcome measure(s)

  • MORTALITY RATE — UP TO 36 MONTHS
    The study will be conducted using electrically insulated composite gloves (Class 2 Starline Linepro insulated gloves) to ensure that chest compressions continue uninterrupted during defibrillation and to determine the effect of this practice on patient survival rates.

Trial sites (1)

FacilityCityRegionStatus
Izmir Katip Çelebi University Izmir Turkey (Türkiye)
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07299188 on ClinicalTrials.gov ↗ ← All trials in Turkey