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Genetic Diseases, Inborn clinical trials

View clinical trials related to Genetic Diseases, Inborn.

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NCT ID: NCT04760314 Completed - Dermatitis, Atopic Clinical Trials

A Study of Lebrikizumab (LY3650150) in Combination With Topical Corticosteroids in Japanese Participants With Moderate-to-Severe Atopic Dermatitis

ADhere-J
Start date: March 10, 2021
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to evaluate the efficacy and safety of lebrikizumab in combination with a topical corticosteroids in Japanese participants with atopic dermatitis.

NCT ID: NCT04594590 Completed - Clinical trials for Mitochondrial Diseases

Natural History Study of SLC25A46 Mutation-related Mitochondriopathy

Start date: November 3, 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of the study is to systematically characterize the clinical course of the progressive neuropathy and optic atrophy observe in pediatric and adult patients with biallelic mutations in the solute carrier family 25 member 46 (SLC25A46) gene.

NCT ID: NCT04584528 Completed - Sickle Cell Disease Clinical Trials

Implementing an Individualized Pain Plan (IPP) for ED Treatment of VOE's in Sickle Cell Disease

ALIGN
Start date: October 27, 2020
Phase: N/A
Study type: Interventional

The overall purpose of this proposed study is to improve management of vaso-occlusive episodes (VOEs) in adult EDs. We aim to implement NHLBI recommendations for VOE treatment by embedding Individualized Pain Plans (IPPs) in the electronic health record (EHR). The EHR-embedded IPP will serve as a record of patients' SCD genotype and will include analgesic medication recommendations developed by the SCD provider. In this project, we will provide access to the IPP for both adult patients with SCD and ED providers. The proposed multisite study will use a pre-post study design, with a core set of mandatory intervention components and strategies for each participating site and optional components and strategies to allow for intervention adaptation to local needs and resources. The EHR-embedded IPP will be available for all adult ED providers to use as their routine practice, and patients will be invited to participate and enroll in the study. We will use a simplified Technology Acceptance Model to explain the use of the IPP and the RE-AIM framework to assess the Reach, Effectiveness, Adoption, Implementation, and Maintenance of the intervention.

NCT ID: NCT04580979 Completed - Clinical trials for Mitochondrial Diseases

Natural History Study of FDXR Mutation-related Mitochondriopathy

Start date: November 3, 2020
Phase:
Study type: Observational [Patient Registry]

The purpose of the study is to systematically characterize the clinical course of the progressive neuropathy and optic atrophy observe in pediatric and adult patients with biallelic mutations in the ferredoxin reductase gene.

NCT ID: NCT04575350 Completed - Genetic Disease Clinical Trials

Reinterpretation of CNV With Unknown Significance: a 5-year Retrospective Analysis

ReAC
Start date: January 1, 2019
Phase:
Study type: Observational

We aim to assess the usefulness of systematic reinterpretation of CNV of unknown significance. To investigate this question we will study all CNV of unknown significance detected between 2010 and 2017.

NCT ID: NCT04556500 Completed - Metabolic Disease Clinical Trials

Turkish Version of the Affordance in the Home Environment for Motor Development-Toddler (AHEMD-T)

Start date: October 1, 2020
Phase:
Study type: Observational

This study aimed to translate the Affordance in the Home Environment for Motor Development -Toddler (AHEMD-T) into Turkish and examine its psychometric properties.

NCT ID: NCT04556487 Completed - Metabolic Disease Clinical Trials

Turkish Affordances in the Home Environment for Motor Development-Infant Scale (AHEMD-IS)

Start date: October 1, 2020
Phase:
Study type: Observational

Environment which children live and grown is very important for the all development stages. In Turkey there is no measurement for home environment evaluation so our aim is to investigate the Psychometric Properties of the Turkish version of Affordances in the Home Environment for Motor Development-Infant Scale (AHEMD-IS) in a sample of Turkısh children.

NCT ID: NCT04420858 Completed - Pregnancy Related Clinical Trials

Effect of Video Education on Patients' Knowledge and Attitudes of Privacy in Prenatal Genetics

Start date: July 21, 2020
Phase: N/A
Study type: Interventional

The investigators propose a randomized controlled trial to assess baseline maternal knowledge of and attitudes toward commercial prenatal genetic testing laboratories' genetic privacy practices, and to determine whether a brief educational intervention alters these attitudes.

NCT ID: NCT04307719 Completed - Clinical trials for Genetic Predisposition

Prevalence of Carriers of Genetic Diseases in the Mexican Jewish Community

Start date: July 1, 2020
Phase:
Study type: Observational [Patient Registry]

The Jewish Population is at an increased risk for genetic diseases, especially autosomal recessive, thus, screening should be done to determine carrier status of several genetic diseases. In the Mexican Jewish Community, which is a very diverse community (regarding geographical origins), data of carrier status is unknown. The study aims to determine carrier prevalence for over 300 diseases using commercially available panels.

NCT ID: NCT03984266 Completed - Genetic Diseases Clinical Trials

The Pilot Study of High-throughput Sequencing in Neonatal Birth Defects

Start date: October 1, 2019
Phase:
Study type: Observational

In China, birth defects can reach as high as 5.6%, about 900,000 new cases of birth defects are added each year, making it the second cause of death for infants, with a total death rate of 19.1%. At present, China implements the three-level prevention and control system for birth defects, which is performed before marriage, before birth, and during the neonatal period. Newborn screening is the last line of defense against birth defects. Early screening diagnosis and timely intervention are extremely important, especially for diseases which can be preventive and treatable. This study aims to evaluate the clinical application of high-throughput targeting sequencing in newborns, and investigate whether this new technology can significantly shorten the time of examination, improve the diagnosis rate, guide the intervention treatments and promote prognosis for these disease.