- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07669103
Bone Cancer Surgery Prospective Database
Bone Cancer Surgery Prospective Database on Perioperative Characteristics and Postoperative Complications
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
At present, there is a lack of high-quality evidence-based measures for perioperative management of bone cancer. Previous studies have mainly been retrospective, with common issues such as missing variables, small sample sizes, and single disease types, making it difficult to systematically reveal perioperative pathophysiological patterns and provide reliable evidence for clinical management. Therefore, high-quality prospective studies are urgently needed.
Therefore, this study intends to conduct a prospective cohort study of patients undergoing surgery for bone cancer, establish a perioperative database, clarify the incidence of complications, explore the factors related to perioperative complications, and provide evidence-based support for improving perioperative management and patient prognosis.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiesteder
-
-
Zhejiang
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Hangzhou, Zhejiang, Kina, 310000
- The Second Affiliated Hospital of Zhejiang University anesthesiology department
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Ledende efterforsker:
- Min Yan, Doctor
-
Kontakt:
- Min Yan, Doctor
- Telefonnummer: +86 15888210247
- E-mail: zryanmin@zju.edu.cn
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Clinical diagnosis of bone cancer
- Scheduled to undergo elective bone cancer resection surgery
Exclusion Criteria:
- Unable to comply with follow-up
- declined participation in the study
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Complication
Tidsramme: hospital discharge, an average of 10 days
|
This includes embolic events, pulmonary complication, wound complication, acute kidney injury, death.
Diagnose according to radiologic examination, sign and symptom
|
hospital discharge, an average of 10 days
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
6 måneders dødelighed
Tidsramme: 6 måneder
|
6 måneder
|
|
|
The rate of perioperative transfusion of allogeneic blood products
Tidsramme: hospital discharge, an average of 10 days
|
This includes blood products such as plasma and platelets, erythrocytes
|
hospital discharge, an average of 10 days
|
|
The coagulation function tests during the perioperative period
Tidsramme: hospital discharge, an average of 10 days
|
This includes thromboelastography result
|
hospital discharge, an average of 10 days
|
|
Wound drainage volume
Tidsramme: hospital discharge, an average of 10 days
|
Accumulated postoperative wound drainage volume
|
hospital discharge, an average of 10 days
|
|
Hemoglobin levels
Tidsramme: hospital discharge, an average of 10 days
|
Hemoglobin levels during hospitalIzation
|
hospital discharge, an average of 10 days
|
|
1-year mortality
Tidsramme: 1 year
|
1 year
|
|
|
2-year mortality
Tidsramme: 2 years
|
2 years
|
|
|
3-year mortality
Tidsramme: 3 years
|
3 years
|
Samarbejdspartnere og efterforskere
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 2026 0873
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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