Cardiac ArrestCODENCT01327833
CODE Registry - Cardiac Arrest Outcomes Data Evaluation
An observational study of Cardiac Arrest, run by Instituto Dante Pazzanese de Cardiologia at 1 site in Brazil.
Trial summary
The purpose of this study is based on method Utstein, registering all recommended items of that model, in addition to adding more information, characterizing this way using a template Utstein modified for the epidemiology of PCR-hospital in Brazil. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cardiac Arrest
- How many people
- Not given
- Where
- 1 siteBrazil
- Study dates
- Start not givento not given
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Adult, Older adult
Study population: Patients in cardiac arrest in-hospital in 17 hospitals and institutes of public and private Brazilian specialties.
Who may be able to join
- Age > 18 years old
- Patient in cardiac arrest in-hospital
- Consent Form signed by subject's legally acceptable representative or by patient in case of survive
Who cannot join
- Patient in cardiac arrest out-hospital
- Cardiac arrest induced (e.g: for cardiac surgery)
Trial locations and contacts
1 site in 1 country.
Brazil1 site
Instituto Dante Pazzanese de Cardiologia
São Paulo, São Paulo, 04012-180
About this study
Official title: Cardiac Arrest Outcomes Data Evaluation
The purpose of this study is based on method Utstein, registering all recommended items of that model, in addition to adding more information, characterizing this way using a template Utstein modified for the epidemiology of PCR-hospital in Brazil.
Objectives: establish a registry of patients suffering from respiratory (PCR)-hospital to assess demographic and clinical variables such as morbidity, mortality and standard practice in cardiopulmonary resuscitation (CPR). In addition, assess independent predictors associated with survival in several times and survival curves.
Read the detailed description
Bedding: Despite of ongoing advances and standardizing worldwide trumpeted by CPR guidelines, yet is little knowledge of the effectiveness of procedures for intra and extra-hospital CPR, so vast are the opportunities for documentation of these results in the field of clinical and epidemiological research. Utstein style emerged, then as a proposed methodology for the PCR during the Conference held at the former monastery Utstein, Norway. The "Utstein Style" was also the model for the construction of the National Registry of Cardiac Pulmonary Resuscitation (NRCPR), sponsored by the American Heart Association (AHA). The proposal of this study is based on method Utstein, registering all recommended items of that model, in addition to adding more information, characterizing this way using a template Utstein modified for the epidemiology of PCR-hospital in Brazil.
Objectives: establish a registry of patients suffering from respiratory (PCR)-hospital to assess demographic and clinical variables such as morbidity, mortality and standard practice in cardiopulmonary resuscitation (CPR). In addition, assess independent predictors associated with survival in several times and survival curves.
Methods: Observational Study of prospective registration type, to document the clinical practice of cardiopulmonary resuscitation in-hospital effect in 17 hospitals and institutes of public and private Brazilian specialties. Additionally the longitudinal follow-up will be conducted until discharged, and measurement of mortality at 6 months and 12 months.
- Conditions
- Cardiac Arrest
- Medical subject headings
- Heart Arrest
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Cardiac Arrest | Not described |
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Apr 2011 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Cardiac ArrestStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Time perspective
- Cross-sectional
Sponsor and investigators
- Lead sponsor
- Instituto Dante Pazzanese de Cardiologia
- Sponsor type
- University, hospital or other
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01327833
- Sponsor's protocol ID
- IDPC-CODE
- Acronym
- CODE
- Status last verified
- Mar 2011
- First submitted
- 31 Mar 2011
- Last updated
- 4 Apr 2011
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 4 Apr 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Cardiac Arrest Outcomes Data Evaluation
- ClinicalTrials.gov ID
- NCT01327833
- Acronym / sponsor ID
- CODE / IDPC-CODE
- Conditions
- Cardiac Arrest
- Study type
- Observational
- Recruitment status
- Completed
- Lead sponsor
- Instituto Dante Pazzanese de CardiologiaUniversity, hospital or other
- First posted
- 4 Apr 2011 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is based on method Utstein, registering all recommended items of that model, in addition to adding more information, characterizing this way using a template Utstein modified for the epidemiology of PCR-hospital in Brazil.
Objectives: establish a registry of patients suffering from respiratory (PCR)-hospital to assess demographic and clinical variables such as morbidity, mortality and standard practice in cardiopulmonary resuscitation (CPR). In addition, assess independent predictors associated with survival in several times and survival curves.
Detailed description
Bedding: Despite of ongoing advances and standardizing worldwide trumpeted by CPR guidelines, yet is little knowledge of the effectiveness of procedures for intra and extra-hospital CPR, so vast are the opportunities for documentation of these results in the field of clinical and epidemiological research. Utstein style emerged, then as a proposed methodology for the PCR during the Conference held at the former monastery Utstein, Norway. The "Utstein Style" was also the model for the construction of the National Registry of Cardiac Pulmonary Resuscitation (NRCPR), sponsored by the American Heart Association (AHA). The proposal of this study is based on method Utstein, registering all recommended items of that model, in addition to adding more information, characterizing this way using a template Utstein modified for the epidemiology of PCR-hospital in Brazil.
Objectives: establish a registry of patients suffering from respiratory (PCR)-hospital to assess demographic and clinical variables such as morbidity, mortality and standard practice in cardiopulmonary resuscitation (CPR). In addition, assess independent predictors associated with survival in several times and survival curves.
Methods: Observational Study of prospective registration type, to document the clinical practice of cardiopulmonary resuscitation in-hospital effect in 17 hospitals and institutes of public and private Brazilian specialties. Additionally the longitudinal follow-up will be conducted until discharged, and measurement of mortality at 6 months and 12 months.
Study design
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cardiac Arrest | – | – |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Patients in cardiac arrest in-hospital in 17 hospitals and institutes of public and private Brazilian specialties.
Key inclusion criteria (3 listed)
- Age > 18 years old
- Patient in cardiac arrest in-hospital
- Consent Form signed by subject's legally acceptable representative or by patient in case of survive
Key exclusion criteria (2 listed)
- Patient in cardiac arrest out-hospital
- Cardiac arrest induced (e.g: for cardiac surgery)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Apr 2011.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cardiac Arrest, run by Instituto Dante Pazzanese de Cardiologia at 1 site in Brazil.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 4 Apr 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Apr 2011; AzTrials last refreshed its copy on 5 Nov 2026.