Instructions

Steps for Participation

1. Access the study protocol.
2. Form a team of up to 3 people to collect data. 
3. Identify an additional local auditor (data monitor, not a surgeon).
4. Register your participation.
5. Read the Frequently Asked Questions (FAQ)
6. Obtain necessary local approvals (if required).
7. Read the instructions on how to use our platform.
8. Submit cases to our electronic Case Report Form (eCRF).

Patient and Center Recruitment is open! 

Information & Instructions

• Join our webinar - Saturday 22 July 2023 14:00 London BST (UTC+1) via zoom
• Read the instructions on how to use our platform.
• Institutional Review Board (IRB) & Ethics
• Patient Information and Consent form (only if required)
• Formation of your local team
• Becoming a country leader
• Authorship
• The study protocol short version in different languages
• Using your desktop, laptop, tablet or smartphone
• Conversion Calculators (height, weight, blood values)
• ASA Status
• Performance Status Scores
• Intraop adverse events
• VAS pain scores
• Clavien-Dindo Classification
• Disclaimer
• Statutes
• Data request form for spinoff studies
• ISRCT Registration (N84544531)

Documents  

• Instructions on how to use our platform (powerpoint) (PDF).
• Short version of the LDLTregistry.org Protocol
• Complete version of the LDLTregistry.org Protocol
• Data Sharing Agreement (NEW, editable)
• Patient Information and Consent form
• Ethics approval (Zurich, Switzerland)
• Audit Committee Approval Certificate of LDLTregistry.org in the UK
• Submission and Case ID database template (excel)
• The LDLTregistry.org Flyer

Video Instructions

General user instructions

 

Case Report Form (CRF) specific instructions

 

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Click here to access the Launch of LDLTregistry.org article.