Ignite Creation Date:
2024-05-06 @ 6:38 PM
Last Modification Date:
2024-10-26 @ 2:52 PM
Study NCT ID:
NCT05738252
Status:
RECRUITING
Last Update Posted:
2024-06-26
First Post:
2023-01-31
Brief Title:
Frailty Assessments for Risk Assessment in Gynecologic Oncology Patients
Sponsor:
Organization:
Population Health Research Institute
Study Design
Study Type:
OBSERVATIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
False
Target Duration:
None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
SAMPLES_WITH_DNA
Bio Spec Description:
Only participants providing specific separate consent will be enrolled in the biobank study We will collect blood samples from patients at baseline ie before and after starting the NACT andor before surgery and then at 28 days after surgery 6 months and 12 months We will collect EDTA tubes to obtain both plasma and whole blood for DNA analysis
Enrollment Count:
280
Enrollment Type:
ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Cohort |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 92752 |
Who Masked List: