registro dei pazienti
Interoperability of Leigh Syndrome Patient Registry Data with Regulatory Submission Standards
Our paper: "Interoperability of Leigh Syndrome Patient Registry Data with Regulatory Submission Standards" is published in the Journal of the Society for Clinical Data Management: https://www.jscdm.org/article/id/244
Leigh Syndrome Global Patient Registry: Uniting Patients and Researchers Worldwide
Our paper: "Leigh Syndrome Global Patient Registry: Uniting Patients and Researchers Worldwide" is published in the Orphanet Journal of Rare Diseases!
To our knowledge this is the first paper about a global patient registry for Leigh syndrome, with many of the reported outcomes reported for the first time. It may also be a first truly international registry in mitochondrial disease with 70% of participants residing outside the United States.
Please read the full paper HERE
Leigh Syndrome Global Patient Registry: Uniting Patients and Researchers Worldwide
Our paper: "Leigh Syndrome Global Patient Registry: Uniting Patients and Researchers Worldwide" is published in the Orphanet Journal of Rare Diseases!
To our knowledge this is the first paper about a global patient registry for Leigh syndrome, with many of the reported outcomes reported for the first time. It may also be a first truly international registry in mitochondrial disease with 70% of participants residing outside the United States.
Please read the full paper HERE
Leigh Syndrome Global Patient Registry
Presented at Euromit, June 2023
To download PDF of the poster in full size please click here.
Building a Worldwide Community - Leigh Syndrome Global Patient Registry
Presented at NORD Rare Diseases and Orphan Products Breakthrough Summit on October 17-18, 2022.
Presented at Mitochondrial Medicine - Therapeutic Development conference in November 2022.
Click HERE to view short overview on YouTube.
To download PDF of the poster in full size please click here.
For a 2 minute video presentation please click here.
Alignment and Interoperability of Leigh Syndrome Registry Data with Regulatory Submission Standards
Presented at PHUSE/FDA Computational Science Symposium, September 2022.
Presented at Mitochondrial Medicine - Therapeutic Development conference in November 2022.
Click HERE to view short overview on YouTube.
Authors: Sophia Zilber, Pallavi Bakare, Kasey Woleben, Saima Kayani, Parag Shiralkar, and Japhanya Bhupathi
Abstract:
The patient data is collected at registries for getting a real-world view of patient reported outcomes, to better understand the disease, and facilitate clinical trials recruitment. Establishment of interoperability of registry data with acceptable submission standards like CDISC is essential in order to accelerate the development of therapies and is a critical milestone in case of rare diseases.
Cure Mito Foundation and Sumptuous Data Sciences, LLC conducted a pilot project for establishment of such interoperability of Leigh Syndrome patient-populated registry data with CDISC standards. This poster presentation provides an overview of the outcome of this pilot project. The poster provides overview of the current data collection practices of patient registry data used by Cure Mito Foundation, provides methodical steps executed to convert such data into CDISC requirements, and provides further assessments regarding conversion of patient-populated data to CDISC and its applicability to other rare disease patient registries.
To download PDF of the poster in full size please click here.
For a 2 minute video presentation please click here.
Registro globale dei pazienti per la sindrome di Leigh
Aiutaci a riunire pazienti, famiglie e ricercatori per ottenere una migliore comprensione della sindrome di Leigh. Se a te o a un membro della tua famiglia è stata diagnosticata in qualsiasi parte del mondo la sindrome di Leigh, iscriviti al registro dei pazienti per dare un contributo importante alla ricerca sulla sindrome di Leigh.
La Cure Mito Foundation sta collaborando con Sanford CoRDS per creare il registro. Sanford CoRDS supporta e consente alle comunità di malattie rare di creare solidi registri, fornendo ai ricercatori le informazioni di cui hanno bisogno per portare avanti la ricerca.
Per ulteriori informazioni sul registro, leggere l'approvazione IRB Domande frequenti .
To hear an audio recording please click below:
%20(60%20%C3%97%2045_205%20in).png)