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 NCT05741983
Ignite Creation Date: 2024-05-06 @ 6:40 PM
Last Modification Date: 2024-10-26 @ 2:52 PM
Study NCT ID: NCT05741983
Protocol Section: NCT05741983
Start Identification Module Data
Expand Identification Module Data
Brief Title: AMIC vs MFx in the Ankle
Official Title: A Prospective Double Blind Single-centre Randomised Controlled Trial Comparing Arthroscopic Autologous Matrix Induced Chondrogenesis AMIC to Microfracture Alone in the Treatment of Osteochondral and Chondral Lesion in the Ankle AMARTA
Acronym: AMARTA
Organization: Geistlich Pharma AG
Organization Class: INDUSTRY
Organization Study ID: 13575-236
Start Status Module Data
Status Verified Date: 2024-03
Overall Status: WITHDRAWN
Study First Submit Date:
Study First Submit QC Date:
Last Update Submit Date:
Status:
Start Sponsor Collaborators Module Data
Investigator:
Lead Sponsor: Geistlich Pharma AG
Lead Sponsor Class: INDUSTRY
Lead Sponsor: Geistlich Pharma AG
Start Oversight Module Data
Description Module:
Study Last Update Post Date Type(Status Module):
Attachment: Upload