- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07669103
Bone Cancer Surgery Prospective Database
Bone Cancer Surgery Prospective Database on Perioperative Characteristics and Postoperative Complications
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
-
-
Zhejiang
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Hangzhou, Zhejiang, China, 310000
- The Second Affiliated Hospital of Zhejiang University anesthesiology department
-
Principal Investigator:
- Min Yan, Doctor
-
Contact:
- Min Yan, Doctor
- Phone Number: +86 15888210247
- Email: zryanmin@zju.edu.cn
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
(1) undergoing elective bone cancer resection surgery.
Exclusion Criteria:
(1)declined participation in the study.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Complication
Time Frame: 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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
6-month mortality
Time Frame: 6 months
|
6 months
|
|
|
The rate of perioperative transfusion of allogeneic blood products
Time Frame: 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
Time Frame: hospital discharge, an average of 10 days
|
This includes thromboelastography result
|
hospital discharge, an average of 10 days
|
|
Wound drainage volume
Time Frame: hospital discharge, an average of 10 days
|
Accumulated postoperative wound drainage volume
|
hospital discharge, an average of 10 days
|
|
Hemoglobin levels
Time Frame: hospital discharge, an average of 10 days
|
Hemoglobin levels during hospitalIzation
|
hospital discharge, an average of 10 days
|
|
1-year mortality
Time Frame: 1 year
|
1 year
|
|
|
2-year mortality
Time Frame: 2 years
|
2 years
|
|
|
3-year mortality
Time Frame: 3 years
|
3 years
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2026 0873
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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