Viewing Protocol Section

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Viewing Protocol Section

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Clinical Trials

To give you an idea of how we make custom software. We have taken all of the Clinical Trials Information from our Federal Government(https://clinicaltrials.gov/).

The JSON File Structure of the files is as follows: Full Study -> Study => Sections => Modules. You are currently viewing a Protocol Section and its Modules.

We give the table structure here to give you an idea of what you are looking at. We put the explanation to the left and the data to the right.

A Protocol Section has the following Modules.

1. Identification Module

2. Status Module

3. Sponsor Collaborators Module

4. Oversight Module

5. Description Module

6. Conditions Module

7. Design Module

8. Arms Interventions Module

9. Outcomes Module

10. Eligibility Module

11. Contacts Locations Module

12. References Module

13. IPD Sharing Statement Module

Viewing Protocol Section

Study NCT06111911
Ignite Creation Date: 2024-05-06 @ 7:43 PM
Last Modification Date: 2024-10-26 @ 3:12 PM
Study NCT ID: NCT06111911
Protocol Section: NCT06111911
Start Identification Module Data
Expand Identification Module Data
Brief Title: Detection of High-Risk HPV in Urine and Cervical Swab Specimen Using HPV Diagnostic Kit Bio Farma
Official Title: Detection of High-Risk Human Papilloma Virus in Urine and Cervical Swab Specimens Comparison Between HPV Diagnostic Kit Bio Farma and COBAS 6800 HPV Roche Molecular Systems
Acronym: None
Organization: PT Bio Farma
Organization Class: INDUSTRY
Organization Study ID: Protokol-BIO-HPV14-BIOFARMA
Start Status Module Data
Status Verified Date: 2023-10
Overall Status: COMPLETED
Study First Submit Date:
Study First Submit QC Date:
Last Update Submit Date:
Status:
Start Sponsor Collaborators Module Data
Investigator:
Lead Sponsor: PT Bio Farma
Lead Sponsor Class: INDUSTRY
Lead Sponsor: PT Bio Farma
Start Oversight Module Data
Description Module:
Study Last Update Post Date Type(Status Module):
Attachment: Upload