Characteristics and Evolution of Hospitalized Patients in Post-Resuscitation Rehabilitation Care Units (SRPR)

NCT ID: NCT03768700

Last Updated: 2023-03-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-03-15

Study Completion Date

2025-08-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Non-interventional cohort study (on data), prospective national multicenter. Inclusion of patients as they enter in a post-intensive care rehabilitation unit (SRPR) .

Collection of data after inclusion, from patients' records during their stay (weekly follow-up) to the SRPR and at their discharge, to D28, D90 and at 1 year after their hospitalization from hospital reports or call of the attending physician.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

For one year, all patients, adults and children hospitalized in a post-intensive care rehabilitation unit (SRPR) of Ile de France and Rouen will be offered to participate in the SRPR Cohort in order to have a completeness of data on a new practice.

The study of these data will make it possible to know the future of the patients and to establish criteria prior to the admission in the SRPR which could make it possible to predict this future and to select the patients as well as possible. It will also make it possible to know the impact of care on the outcome of patients at discharge, at 28 days, 90 days and 1 year of their admission to SRPR to improve practices.

This research will focus on the collection of data from patients' medical records. General information about their stay in the intensive care unit - including the patient's ventilatory status - will be collected upon arrival at the SRPR units, during their stay (weekly follow-up), at the exit of the SRPR, at D28, and in the longer term. (J90 and J365 of the entry into the SRPR unit) where will be listed more comprehensive data with, in addition to general information, data on nutritional, neurological, neuromuscular, respiratory and biological hemodynamic assessments will be collected.

In addition to the common data base, each type of SRPR (respiratory and pediatric neurology) will collect data that is specific to its specialty.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hospitalization in a Post-Resuscitation Rehabilitation Care Units

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Cohort

Hospitalization in a Post-Resuscitation Rehabilitation Care Units (SRPR)

Data gathering

Intervention Type OTHER

Questionnaires and collection of medical data on patients during hospitalization, at D28, at 90 and at 1 year

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Data gathering

Questionnaires and collection of medical data on patients during hospitalization, at D28, at 90 and at 1 year

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Hospitalization in a Post-Resuscitation Rehabilitation Care Units (SRPR) of Ile de France and Rouen

Exclusion Criteria

* Refusal of access to the data by the patient or the designated trusted person or the holder (s) of parental authority (pediatric population)
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Alexandre DEMOULE, Pr

Role: PRINCIPAL_INVESTIGATOR

Hôpital Pitié-Salpêtrière - AP-HP

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Groupe hospitalier des portes de l'Oise

Beaumont-sur-Oise, , France

Site Status NOT_YET_RECRUITING

Centre hospitalier de Bligny

Briis-sous-Forges, , France

Site Status NOT_YET_RECRUITING

Hôpital d'instruction des armées - Percy

Clamart, , France

Site Status NOT_YET_RECRUITING

Hôpital de Forcilles

Férolles-Attilly, , France

Site Status NOT_YET_RECRUITING

Hôpital Raymond Poincaré - SRPR pédiatrique

Garches, , France

Site Status NOT_YET_RECRUITING

Hôpital Raymond Poincaré de Garches - SRPR neurologique

Garches, , France

Site Status NOT_YET_RECRUITING

Hôpital Bicêtre

Le Kremlin-Bicêtre, , France

Site Status NOT_YET_RECRUITING

Hôpital Pitié-Salpêtrière

Paris, , France

Site Status RECRUITING

Hôpital Sainte-Anne

Paris, , France

Site Status NOT_YET_RECRUITING

Hôpital Charles-Nicolle - CHU de Rouen

Rouen, , France

Site Status NOT_YET_RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

France

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Alexandre DEMOULE, Pr

Role: CONTACT

0142167727

Julie DELEMAZURE, Dr

Role: CONTACT

0184827572

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Eric BOUDET, Dr

Role: primary

Henry MAAS, Dr

Role: primary

David ROGEZ, Dr

Role: primary

Laurence DONETTI, Dr

Role: primary

Blaise MBIELEU, Dr

Role: primary

Julie PAQUEREAU, Dr

Role: primary

Bernard VIGUE, Dr

Role: primary

Alexandre DEMOULE, Pr

Role: primary

0142167727

Julie DELEMAZURE, Dr

Role: backup

0184827572

Florence COLLE, Dr

Role: primary

Gaëtan BEDUNEAU, Dr

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2018-A00743-52

Identifier Type: OTHER

Identifier Source: secondary_id

NI17008J

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.