- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT05170321
Analysis of Influencing Factors and Construction of Prediction Models of Artificial Joint Replacement in China
30 décembre 2021 mis à jour par: Xiangya Hospital of Central South University
The project intends to analyze the epidemiological characteristics, risk factors, complications and resource utilization of artificial joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The HQMS database is a mandatory electronic inpatient database system developed by the National Health Commission of the People's Republic of China.
Since 2013, tertiary hospitals have been required to upload their inpatient discharge records.
By 2019, the HQMS database has included more than 230 million standardized inpatient discharge records of over 1000 hospitals across all 31 provincial-level administrative regions in mainland China.
Patient demographics, clinical diagnosis, procedures and operations, drug use, costs and complications were all recorded in the HQMS database.
The investigators planned to include five types of arthroplasty, including knee arthroplasty, hip arthroplasty, shoulder arthroplasty, ankle arthroplasty and elbow arthroplasty.
The data analysis will be conformed to the principle of confidentiality and will not reveal the privacy of those patients.
The data will be only used for this research project and there is no conflict of interest.
It is in line with the principles of ethics, harmlessness and fairness.
This study was authorized by the HQMS Committee Board and approved by the institutional review board, with waiver of informed consent.
Aperçu de l'étude
Statut
Actif, ne recrute pas
Type d'étude
Observationnel
Inscription (Anticipé)
600000
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Hunan
-
Changsha, Hunan, Chine, 410008
- Xiangya Hospital of Central South University
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
Méthode d'échantillonnage
Échantillon non probabiliste
Population étudiée
Patients who underwent knee, hip, shoulder, ankle and elbow arthroplasty were included.
La description
Inclusion Criteria:
- Patients who underwent knee, hip, shoulder, ankle and elbow arthroplasty in HQMS
Exclusion Criteria:
- Patients who didn't undergo knee, hip, shoulder, ankle and elbow arthroplasty
- Patients with missing demographics or medical data
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
---|
patients undergoing knee arthroplasty in Hospital Quality Monitoring System in China
Patients who underwent knee arthroplasty and was recorded in HQMS were included in this group
|
patients undergoing hip arthroplasty in Hospital Quality Monitoring System in China
Patients who underwent hip arthroplasty and was recorded in HQMS were included in this group
|
patients undergoing shoulder arthroplasty in Hospital Quality Monitoring System in China
Patients who underwent shoulder arthroplasty and was recorded in HQMS were included in this group
|
patients undergoing ankle arthroplasty in Hospital Quality Monitoring System in China
Patients who underwent ankle arthroplasty and was recorded in HQMS were included in this group
|
patients undergoing elbow arthroplasty in Hospital Quality Monitoring System in China
Patients who underwent elbow arthroplasty and was recorded in HQMS were included in this group
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Epidemiological characteristics, complications, risk factors and resource utilization of knee arthroplasty in China
Délai: 10 years (2013-2022)
|
The project intends to analyze the epidemiological characteristics, complications, risk factors and resource utilization of artificial knee joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The information collected by HQMS includes demographics characteristics, hospitalization information, medical care cost, complications, et al.
|
10 years (2013-2022)
|
Epidemiological characteristics, complications, risk factors and resource utilization of hip arthroplasty in China
Délai: 10 years (2013-2022)
|
The project intends to analyze the epidemiological characteristics, complications, risk factors and resource utilization of artificial hip joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The information collected by HQMS includes demographics characteristics, hospitalization information, medical care cost, complications, et al.
|
10 years (2013-2022)
|
Epidemiological characteristics, complications, risk factors and resource utilization of shoulder arthroplasty in China
Délai: 10 years (2013-2022)
|
The project intends to analyze the epidemiological characteristics, complications, risk factors and resource utilization of artificial shoulder joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The information collected by HQMS includes demographics characteristics, hospitalization information, medical care cost, complications, et al.
|
10 years (2013-2022)
|
Epidemiological characteristics, complications, risk factors and resource utilization of ankle arthroplasty in China
Délai: 10 years (2013-2022)
|
The project intends to analyze the epidemiological characteristics, complications, risk factors and resource utilization of artificial ankle joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The information collected by HQMS includes demographics characteristics, hospitalization information, medical care cost, complications, et al.
|
10 years (2013-2022)
|
Epidemiological characteristics, complications, risk factors and resource utilization of elbow arthroplasty in China
Délai: 10 years (2013-2022)
|
The project intends to analyze the epidemiological characteristics, complications, risk factors and resource utilization of artificial elbow joint replacement in China through the inpatient data collected by the Hospital Quality Monitoring System (HQMS).
The information collected by HQMS includes demographics characteristics, hospitalization information, medical care cost, complications, et al.
|
10 years (2013-2022)
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Les enquêteurs
- Chercheur principal: Guanghua Lei, PhD; MD, Xiangya Hospital
Publications et liens utiles
La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 janvier 2018
Achèvement primaire (Anticipé)
1 décembre 2022
Achèvement de l'étude (Anticipé)
1 décembre 2022
Dates d'inscription aux études
Première soumission
8 décembre 2021
Première soumission répondant aux critères de contrôle qualité
8 décembre 2021
Première publication (Réel)
27 décembre 2021
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
14 janvier 2022
Dernière mise à jour soumise répondant aux critères de contrôle qualité
30 décembre 2021
Dernière vérification
1 novembre 2021
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2017121016
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Description du régime IPD
The investigators do not wish to share our data according to the policy of our hospital, the data could not be shared with others without permission.
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .