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Congenital Abnormalities clinical trials

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NCT ID: NCT04514939 Not yet recruiting - Leg Edema Clinical Trials

Elevate to Alleviate Evidence Based Study

ETA
Start date: September 1, 2020
Phase:
Study type: Observational

Venous return in the circulatory system of lower limbs results from the interaction of several mechanisms, and reflects the balance between blood inflow and outflow. Blood outflow improves during sleeping because of the lying position especially with leg elevation. In fact, patients with chronic venous disease (CVD) improve leg symptoms in lying position and with leg elevation. The aim of this study is to evaluate the level of comfort of hospital inpatients, without CVD, if they lie with a moderate leg elevation during hospital stay.

NCT ID: NCT04512118 Completed - Clinical trials for Presence of COVID-19 Compatible CT Abnormalities

CT Abnormalities Evocative of Lung Infection Are Associated With Lower 18F-FDG Uptake in Confirmed COVID-19 Patients

Start date: March 15, 2020
Phase:
Study type: Observational

CT signs that are evocative of lung COVID-19 infections have been extensively described, whereas 18F-FDG-PET signs have not. Our current study aimed to identify specific COVID-19 18F-FDG-PET signs in patients that were (i) suspected to have a lung infection based on 18F-FDG-PET/CT recorded during the COVID-19 outbreak and (ii) whose COVID-19 diagnosis was definitely established or excluded by appropriate viral testing.

NCT ID: NCT04504682 Terminated - Obesity Clinical Trials

Ambulation With Labor Epidural in Obese Women

Start date: August 25, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if ambulation with a labor epidural in place is associated with decreased rate of cesarean delivery in obese patients.

NCT ID: NCT04503759 Completed - Trauma Injury Clinical Trials

Artoss Foot and Ankle Surgery Registry

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

This prospective registry was designed as an observational study to ascertain how commercially available NanoBone products are being used by surgeons performing foot and ankle surgery which involves bone grafting, as well as determining relevant patient outcomes.

NCT ID: NCT04501003 Recruiting - Infertility, Female Clinical Trials

Investigation of U1-A Uterine Anomalies Implantation Markers From the Lateral Walls of the Endometrium

Start date: December 12, 2019
Phase: N/A
Study type: Interventional

Various types and classes of uterine malformations have been identified and the ESHRE / ESGE classification system has recently been published on female genital system anomalies. Postoperative positive pregnancy results were obtained in studies conducted in patients with infertility, recurrent implantation failure, and recurrent pregnancy loss, which were not previously described in T-shaped uterine anomalies. Considering the increase in endometrial gland and vascularity after the surgical procedure performed in these patients, our primary goal in our study is to compare the number of implantation markers (αVβ3 integrin) and subepithelial glands in the specimen biopsies taken from the lateral walls of the endometrium before and after hysteroscopic surgery in patients with class U1a anomalies.

NCT ID: NCT04491812 Recruiting - Deformity Flexion Clinical Trials

Triceps Taping on Elbow Flexion Tightness in Extended Erb's Palsy

Start date: August 10, 2020
Phase: N/A
Study type: Interventional

To determine the role of using Kinesiology tape on the prevention of elbow flexion tightness in infants with extended Erb's palsy.

NCT ID: NCT04486794 Completed - Clinical trials for Tear Trough Eyelid Deformity

Restylane® for the Treatment of Tear Trough Deformity

Start date: July 7, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effectiveness and tolerability of Restylane® for correction of tear trough deformity, using various injection techniques.

NCT ID: NCT04486599 Completed - Venous Malformation Clinical Trials

Electromagnetic Navigation During Ultrasound Guided Foam Sclerotherapy for Venous Malformations

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

The aim of this study is to evaluate the feasibility of assisted electromagnetic navigation in percutaneous echo-guided sclerotherapy of slow-flow vascular malformations. Feasibility will be defined in terms of the percentage of patients for whom the procedure is successful.

NCT ID: NCT04475289 Recruiting - Clinical trials for Anomalous Coronary Artery Origin

Registry for Invasive and Non-invasive Anatomical Assessment and Outcome of Coronary Artery Anomalies

NARCO
Start date: January 1, 2000
Phase:
Study type: Observational [Patient Registry]

An anomalous coronary artery from the opposite sinus of Valsalva (ACAOS) represents a congenital disorder with an anomalous location and/or course of the coronary vessel. The prevalence of ACAOS in the general population is around 1 % and they are mostly clinically insignificant and remain often undetected. However, some variants of ACAOS are associated with adverse cardiac events. The possible presence of an interarterial/intramural course is the primary cause for an oval proximal vessel shape and/or proximal vessel narrowing, which may lead under stress conditions to a "dynamic compression" of the vessel (compared to "fixed" stenosis in coronary artery disease). To mimic these conditions, dobutamine and volume challenge is used to invasively measure fractional flow reserve (FFR) during coronary angiography and is seen as the gold standard in assessing the hemodynamic relevance of ACAOS. We established a specialized interdisciplinary clinic for coronary artery anomalies including imaging specialists, invasive cardiologists and congenital heart disease surgeons as correct downstream testing and treatment decision is highly challenging in these patients. Thus, systematic collecting of all available diagnostic methods (invasive and non-invasive) is required to assess the optimal diagnostic procedure and treatment for these patients. Coronary computed tomography angiography (CCTA) is the method of choice to characterize the exact anatomy of ACAOS. However, how functional invasive FFR is associated with anatomical CCTA findings is unknown. Further, diagnostic accuracy of a novel independent research algorithm with computational fluid dynamics (ctFFR) as well as functional imaging (i.e. stress single photon emission computed tomography) in this specific setting is unknown. The presented project will help to understand the pathophysiology of CAAs with particular focus on ACAOS-IC and improve risk stratification based on non-invasive imaging.

NCT ID: NCT04471259 Completed - Haglund's Deformity Clinical Trials

Functional Follow-up After Endoscopic Calcaneoplasty for Haglund's Deformity

Start date: January 22, 2012
Phase:
Study type: Observational

Isokinetic muscle strength test implemented by the Biodex system is a method used for evaluating muscle function that has been applied clinically in the field of sports and rehabilitation medicine. However, information on its application on Haglund's deformity remain insufficient. Therefore, the present study is designed to examine the effectiveness of the muscle strength test using the Biodex system in evaluating the recovery of athletic capacity in patients with Haglund's deformity following endoscopic surgery.