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Congenital Abnormalities clinical trials

View clinical trials related to Congenital Abnormalities.

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NCT ID: NCT04303949 Not yet recruiting - Clinical trials for Termination of Pregnancy

Multi-Media E-Book for Second‐Trimester Termination Due to Fetal Anomaly

Start date: March 20, 2020
Phase: N/A
Study type: Interventional

The subjects of this study are married couples who received termination of pregnancy, the main purpose is to explore the effectiveness of the e-book education model. Outcome indicators include anxiety, depression, and grief, as well as the satisfaction of the education.

NCT ID: NCT04298216 Not yet recruiting - Clinical trials for Inferior Vena Cava Abnormality

Transhepatic Versus Subcostal Views to Assess Inferior Vena Cava Variation in Pediatric Patients

Start date: January 2024
Phase: N/A
Study type: Interventional

Currently, in order to visualize the inferior vena cava (IVC) of the heart using ultrasound, physicians traditionally place the ultrasound probe onto the "Subcostal" area which is located below the chest in the upper abdomen area. In this location, the pressure from the ultrasound probe is often uncomfortable for adults, and even more so for pediatric patients. Previous research and physician experience have demonstrated that it is possible to visualize the heart in the "transhepatic" area which is located under the arm on the side of the chest. By placing the ultrasound probe in this location, it is more comfortable for the patient when applying pressure, and this study aims to prove the effectiveness of visualizing the heart through this new location.

NCT ID: NCT04297033 Not yet recruiting - Clinical trials for Cerebral Arteriovenous Malformation

Lovastatin for Treatment of Brain Arteriovenous Malformations

Start date: January 1, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this pilot study is to evaluate the disease-modifying efficacy of lovastatin in patients with brain arteriovenous malformation.

NCT ID: NCT04293302 Completed - Brain Abnormalities Clinical Trials

Early Postnatal Management of Gestational Brain Sonographic Malformations.

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

Gestational sonographic follow up may find some brain malformations. The trial is about to characterize these findings and correlate with the immediate postnatal findings.

NCT ID: NCT04286360 Recruiting - RAS Mutation Clinical Trials

Hematological Anomalies in Children With Rasopathy

RAS-HEMATO
Start date: November 11, 2020
Phase:
Study type: Observational

During childhood, patients with RASopathies (Noonan syndrome and related diseases) can harbor various hematological anomalies ranging from isolated monocytosis, myelemia, thrombocytopenia or splenomegaly to myeloproliferative disorders. These anomalies may spontaneously disappear or persist, sometimes leading to juvenile myelomonocytic leukemia. Guidelines for initial screening and subsequent hematological follow-up have recently been published in France: peripheral blood analysis should be performed in all newly diagnosed patients and followed by biannual peripheral blood analysis in infants until the age of 2 years. In order to describe the characteristics of these abnormalities in terms of their incidence, age of occurrence, evolution and relation to genotype, we are conducting a longitudinal prospective study whose aim is to analyze peripheral blood cell counts and smears at diagnosis and one year later. In patients <3 years of age recruited at certain centers, biobanking of mononuclear cells will be performed. These data could yield a new insight into hematological anomalies in patients with RASopathies and thereby help physicians to determine the appropriate rhythm for hematological follow-up according to genotype.

NCT ID: NCT04282408 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Experimental Evaluation of Back Braces for the Treatment of Spinal Deformity Produced With 3D Printing Technology

Start date: July 9, 2019
Phase: N/A
Study type: Interventional

The proposed investigation is a pilot study that involves pediatric patients affected by spinal deformity (Adolescent Idiopathic Scoliosis and Osteogenesis Imperfecta). The main goal is to evaluate the acceptability, the safety and the overall satisfaction of the patients wearing the back braces produced with an innovative methodology using 3D printers, compared to the current braces manufactured with a production model based on thermoforming, that has well-established clinical efficacy.

NCT ID: NCT04271722 Completed - Clinical trials for Labor Onset and Length Abnormalities

Clinical Evaluation of Cervical Ripening in the Outpatient Setting

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

A randomized controlled trial of mifepristone 200mg vs balloon catheter for cervical ripening.

NCT ID: NCT04263935 Recruiting - Lymphoma Clinical Trials

Correlation Between Driver Gene Abnormalities and Clinicopathological Characteristics and Disease Prognosis in Lymphoma

Start date: January 3, 2019
Phase:
Study type: Observational

Correlation Between Driver Gene Abnormalities and Clinicopathological Characteristics and Disease Prognosis in Lymphoma

NCT ID: NCT04258046 Recruiting - Arterial Disease Clinical Trials

Trametinib in the Treatment of Complicated Extracranial Arterial Venous Malformation

Start date: December 1, 2020
Phase: Phase 2
Study type: Interventional

Arteriovenous malformation (AVM) is a congenital vascular anomaly that progresses throughout life and causes complications including tissue destruction due to rapid overgrowth, bleeding, functional deficits, severe deformity and cardiac failure. Unfortunately, traditional managements have transient benefits with more than 90 recurrence rate within a year. Therefore, there is a significant unmet medical need. The purpose of this study is to assess the safety and efficacy of Trametinib in children and adults with Extracranial Arteriovenous Malformation (AVM).

NCT ID: NCT04249791 Recruiting - Uterine Anomaly Clinical Trials

Laparoscopic-robotic Hysterectomy for Uterine Transplantation in Live-donor Patient.

transplant
Start date: June 25, 2019
Phase: N/A
Study type: Interventional

Currently, there is no standard and indicated standard access route for uterine removal in the uterine transplant donor patient. The aim of the study is to show the feasibility of performing this procedure by replicating in our center the results found in other recent studies and to try to reduce the surgery time for both the donor and recipient patients.