Design Module
The Design Module contains detailed information about the study design, including study type, allocation methods, intervention models, masking information, primary purpose, enrollment details, and biospecimen information. This module provides essential details about how the clinical trial is structured and conducted.
Design Module path is as follows:
Study -> Protocol Section -> Design Module
Design Module
Ignite Creation Date:
2025-12-26 @ 10:19 PM
Ignite Modification Date:
2025-12-26 @ 10:19 PM
NCT ID:
NCT05975112
Study Type:
OBSERVATIONAL
Study:
NCT05975112
Study Brief:
The Incidence of Hyperfibrinolysis During Vaginal Delivery and Cesarean Section
Protocol Section:
NCT05975112
Bio Specs (If Any):
Bio Specs
| Retention | Description | View |
|---|---|---|
| SAMPLES_WITH_DNA | one blood sample of 6ml | View |
Design Masking Infos (If Any):
Design Observational Models (If Any):
Design Time Perspectives (If Any):
Design Who Masked (If Any):
Enrollment Infos (If Any):
Enrollment Infos
| Enrollment Type | Enrollment Count | View |
|---|---|---|
| ESTIMATED | 780 | View |
Expanded Access Types (If Any):
Phases (If Any):