Examining how frailty affects outcomes of CPR in patients needing emergency response
The Impact of Frailty on Cardiopulmonary Resuscitation Adverse Outcomes in Patients Requiring Code Blue Activation
This study looks at how frailty affects the chances of survival after CPR in older patients who need emergency help.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 2 (estimated) |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Sponsor | Umraniye Education and Research Hospital Government |
| Locations | 2 sites (Istanbul, Umraniye and 1 other locations) |
| Trial ID | NCT06405581 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the relationship between frailty and the outcomes of cardiopulmonary resuscitation (CPR) in patients who trigger a code blue response. It focuses on understanding how various factors, including patient age and physiological conditions, influence survival rates during in-hospital cardiac arrests. The study utilizes the Edmonton frailty scale to assess frailty levels among participants, particularly in the elderly population. By analyzing these associations, the research seeks to provide insights that could improve emergency response protocols.
Who should consider this trial
Good fit: Ideal candidates for this study include elderly patients, particularly those aged 65 and older, who may be experiencing frailty.
Not a fit: Patients who are pregnant or those who do not meet the frailty criteria may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the effectiveness of CPR interventions in frail patients, potentially improving survival rates.
How similar studies have performed: While there is ongoing research into the impact of frailty on health outcomes, this specific focus on CPR outcomes in frail patients is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * pediatric patients Exclusion Criteria: * pregnant patients
Where this trial is running
Istanbul, Umraniye and 1 other locations
- Umraniye Education and Research Hospital — Istanbul, Umraniye, Turkey (Türkiye) (Recruiting)
- Umraniye Education and Research Hospital — Istanbul, Umraniye, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: ZELİHA TUNCEL, ass prof
- Email: zelihalara@yahoo.com
- Phone: +905053577483
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.