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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT05456048 Completed - Clinical trials for Refractory Acute Myeloid Leukemia

Influence of Molecular Abnormalities on Response of VAH vs. VEN+HMA in RR-AML

Start date: December 3, 2018
Phase:
Study type: Observational

The aim of this study is to reveal the influence of gene mutations on the treatment response of the regimen of HHT combined with Venetoclax plus AZA versus venetoclax plus HMA in the salvage therapy of RR-AML.

NCT ID: NCT05438433 Completed - Clinical trials for Mitral Valve Replacement

Outcome of Preserved Mitral Valve Apparatus During Mitral Valve Replacement

EarlyOutcome
Start date: December 28, 2016
Phase: N/A
Study type: Interventional

Are there differences in outcome of mitral valve replacement with preservation of mitral apparatus among rheumatic and/or ischemic mitral lesions?. Mitral valve replacement with preservation of leaflets, and added coronary artery-bypass surgery, when indicated, is it a feasible and reproducible procedure?. The study was designed to compare outcome after prosthetic mitral replacement with preservation of mitral apparatus for rheumatic valve disease with outcome of replacement for ischemic myocardium and mitral valve disease, The outcomes will be guided by clinical assessment. and echo-cardiograph.

NCT ID: NCT05437042 Completed - Foot Deformities Clinical Trials

Effect of Medial Wedge on Static Balance in Pronated Feet

Start date: April 1, 2021
Phase:
Study type: Observational

The use of heel wedges is often recommended as a clinical routine in individuals with foot pronation. However, there is a lack of information for examining the immediate effect of supports used to restore foot biomechanics on balance. The aim of our study is to examine the immediate effect of calcaneal support in the frontal plane on static balance in individuals with increased pronated foot. In this study, the fore-hind foot load distribution in static bipedal stance will be examined in healthy young adults. Then, static balance measurements will be made on one leg with and without support (medial heel wedge). For the evaluation of static balance on one leg, x-y mean, ellipse surface, A-P index measurements and romberg test will be used. In addition, the pain of individuals will be questioned and their foot postures will be evaluated. Healthy young adult individuals with a subtalar angle of 5 degrees and above in the weighted position will be included in the evaluations. Evaluations of the participants are planned to take approximately 15 minutes.

NCT ID: NCT05412420 Completed - Solid Tumor Clinical Trials

Artificial Intelligence to Search for Abnormalities in Ambulatory Cancer Patients

IASAAC
Start date: August 3, 2022
Phase: N/A
Study type: Interventional

During treatment, cancer patients may experience side effects related to their disease but also to the different treatments they receive. Currently, adverse effects and toxicities are well codified in the oncology community, notably via the NCI CTCAE criteria. Unlike objective data such as a blood sample or a CTscan, a major bias in patient assessment is the subjective assessment of the physician or its team at a given time, which may not reflect the overall situation (for better or worse). Several studies had already highlighted the discrepancies between medical and patient data collection. Self-assessment of symptoms is one way to overcome this bias. Moreover, there are now a large number of solutions that allow to perform these self-assessments at home. Thanks to these tools, there are now two situations, the scheduled evaluation (before a chemotherapy treatment, or after a surgical procedure for instance) and the unscheduled situations, where it is the patient himself who can trigger an evaluation form. These new evaluation methods also allow to take a quality of life approach. Patient-reported outcomes (PROs) is now a valid evidence-based assay to detect patient's symptoms and therefore provide helpful clinical information to healthcare providers. The goal of this study is to go one step further than the previous PROs studies and evaluate the ability to train a machine learning algorithm to detect at-risk situations and lay the foundation for a viable solution for future prospective and randomized trials.

NCT ID: NCT05369247 Completed - Pregnancy Related Clinical Trials

Interval Versus Continuous Exercise During Pregnancy

Start date: December 1, 2020
Phase: N/A
Study type: Interventional

The objective of this randomized cross-over design was to investigate the fetal well-being and maternal glycemic response to an acute bout of aerobic high-intensity interval training (HIIT) and moderate-intensity continuous training (MICT) with pregnant individuals.

NCT ID: NCT05349942 Completed - Palate; Deformity Clinical Trials

A Digital Method for Measurement of Palatal Asymmetry in Twins

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

The aim of the study is to evaluate the digital palatal model as a possible tool of human identification.

NCT ID: NCT05318222 Completed - Clinical trials for Neurodevelopmental Disorders

Genetic Inclusion by Virtual Evaluation

GIVE
Start date: June 1, 2022
Phase: N/A
Study type: Interventional

This study aims to transform the current clinical practice paradigm by leveraging an internally designed web-based model of delivery of care called Consultagene to provide remote evaluation and genomic sequencing for improving genetic health of less resourced children with rare disorders living along the Texas-Mexico border.

NCT ID: NCT05306483 Completed - Clinical trials for Heart Defects, Congenital

Transcatheter Versus Surgical Closure of Ventricular Septal Defect: A Comparative Study

Start date: June 12, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare Safety, efiicacy and clinical effects of surgical versus transcatheter closure of ventricular septal defect (VSD ). The outcome of interest is success rate, residual shunts, effect on tricuspid and aortic valves, need for blood transfusion, length of hospital and intensive care unit ( ICU ) stay, complications especially complete heart block, affection of kidney functions due to the procedure length caused by Cardiopulmonary bypass in case of surgical group or by the dye used in the group of transcatheter closure.

NCT ID: NCT05282368 Completed - Clinical trials for Parent Mental Health

Preparing Heart and Mind™: A Patient Engagement Pathway for Parents and Their Caregiving Partners After a Major Fetal Anomaly Diagnosis

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to test and evaluate the Preparing Heart and Mind™ (PHM™) patient engagement pathway as a nurse-guided intervention to lower psychological distress and enhance caregiving competencies among mothers/birthing persons and their caregiving partners after a major fetal anomaly diagnosis.

NCT ID: NCT05258695 Completed - Orthopedic Disorder Clinical Trials

The Turkish Version of the AOFAS Hallux MTP-IP

Start date: July 15, 2021
Phase:
Study type: Observational

The American Orthopedic Foot and Ankle Society hallux metatarsophalangeal-interphalangeal joint scale (AOFAS Hallux MTP-IP) is originally developed in English to evaluate the pain, function and alignment in patients with hallux deformities. The purpose of this study is to translate and cross-culturally adapt the AOFAS Hallux MTP-IP scale into Turkish and investigate its psychometric properties.