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NCT ID: NCT04331496 Recruiting - Bronchiolitis Clinical Trials

Saline vs Hypertonic Serum With Respiratory Physiotherapy in a Recurrent Wheezing Patient

Start date: April 4, 2020
Phase: N/A
Study type: Interventional

Bronchiolitis (BQ) is an acute viral infection of the lower respiratory tract that affects the bronchioles of babies younger than 24 months of age. Respiratory physiotherapy (FTR) appears as a complementary treatment measure in clinical guidelines and consensus on the management of BQ. Nebulization with 3% hypertonic serum before the FTR session induces an osmotic flow of water in the mucus, which facilitates drainage and reduces edema in the submucosal tissue.

NCT ID: NCT04330898 Recruiting - Clinical trials for Implantable Cardiac Device. Patients With a NMR Indication

Patients With Implantable Cardiac Devices Requiring a Nuclear Magnetic Resonance

RESONANCE
Start date: May 2, 2017
Phase:
Study type: Observational [Patient Registry]

The general objective of this registry is to study the number of patients carrying an implantable cardiac device that have an indication for an imaging diagnosis based on nuclear magnetic resonance. Is wanted to know the cause of the indication of the diagnostic test based on MRI.

NCT ID: NCT04330846 Recruiting - Crohn Disease Clinical Trials

Prospective Multicenter Randomized Comparative Study of the Treatment of de Novo Stenosis in Chron's Disease.

ENDOCIR
Start date: November 29, 2022
Phase: N/A
Study type: Interventional

Stenosis is one of the most frequent complications in patients with Crohn's disease (CD), causing greater morbidity and increasing the probability of repeated surgery and short bowel syndrome (1-3). Endoscopic balloon dilation (EBD) is clearly the treatment of choice for short stenoses located at the anastomosis of previous surgeries (4-6). However, there is no scientific evidence for determining the most appropriate treatment for de novo stenosis less than 10 cm in length (surgical versus endoscopic treatment), both in terms of efficacy and complications. Neither has it been established which of these two approaches has a greater impact on the quality of life of patients and on costs.

NCT ID: NCT04328051 Recruiting - Clinical trials for Bacterial Infections

Influence of the Implant-prosthetic Connection in the Marginal Bone Loss and Bacterial Leakage

Start date: June 13, 2018
Phase: N/A
Study type: Interventional

This study consists in a double-blinded randomized controlled trial which objective is to assess the effect of the implant-abutment connection type -external hexagon, internal hexagon and conical connection- in the periimplant marginal bone loss in vertical side and the bacterial leakage 12 months after prosthesis placement.

NCT ID: NCT04326400 Recruiting - Clinical trials for Coronavirus Infection

Active Monitoring And Determinants of Incidence Infection of COVDI-19

Start date: March 23, 2020
Phase:
Study type: Observational

7. Objectives To apply e-health methods to perform active monitoring and assess determinants of incident Infection of COVID-19 in a hospital population. 8. Study design Prospective, Single-centre, observational clinical study. 9. Disease or disorder under study Healthy people in risk of COVID-19 infection. 10. Main variable. Symptoms related to infection caused by SARS-Cov2. 11. Study population and total number of patients Men and women in general god health status aged between 18 and 80 years that currently are employees of Hospital de La Princesa . 12. Duration of treatment Each subject will be monitored, since its recruitment, for a period of 12 weeks. 13. Timetable and expected date of completion The overall duration of the study is estimated at about 6 months, from patient recruitment to the last data recorded by last subject. The aim is to carry out this study from March 2020 onwards.

NCT ID: NCT04323644 Recruiting - COVID-19 Clinical Trials

Outcomes of Surgery in COVID-19 Infection: International Cohort Study (CovidSurg)

CovidSurg
Start date: January 1, 2020
Phase:
Study type: Observational

CovidSurg will capture real-world international data, to determine 30-day mortality in patients with COVID-19 infection who undergo surgery. This shared international experience will inform the management of this complex group of patients who undergo surgery throughout the COVID-19 pandemic, ultimately improving their clinical care.

NCT ID: NCT04321018 Recruiting - Metabolic Syndrome Clinical Trials

Effect of a Mixed Macronutritional Meal With Medium Chain Triglycerides on the Oxidation of Postprandial Macronutrients

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

The main aim of this study is to determine the effect of the addition of medium chain triglycerides to a mixed macro nutritional meal on postprandial macronutrients oxidation (i.e. fat oxidation, carbohydrate oxidation, change in respiratory quotient, peak respiratory quotient, etc.).

NCT ID: NCT04320433 Recruiting - Glucose Intolerance Clinical Trials

Inter-day Reliability of the Oral Glucose Tolerance Test Using Indirect Calorimetry

Start date: April 2020
Phase: N/A
Study type: Interventional

The main aim of this study is to determine the inter-day reliability, by using indirect calorimetry, of the post-prandial macronutrient oxidation and energy expenditure after consuming oral glucose load solution.

NCT ID: NCT04314869 Recruiting - Sterility, Female Clinical Trials

Uterus Transplantation Procedure From a Live Donor

Start date: May 23, 2020
Phase: N/A
Study type: Interventional

Absolut uterine factor, meaning the absence of uterus, represents a cause for sterility without the possibility of a present treatment. The uterine factor affects millions of women and may be due to congenital problems, such as the Muller anomalies (Mayer Rockitansky Syndrome) or acquired by previous hysterectomy or intrauterine adhesions (Asherman's Syndrome). The uterine transplant would represent the only possibility for patients with an absolute uterine factor to achieve both genetic and gestational maternity.

NCT ID: NCT04314557 Recruiting - Hypertension Clinical Trials

Renal Arterial Denervation in Sympathetic Dysautonomia

RANSOM
Start date: March 14, 2019
Phase:
Study type: Observational [Patient Registry]

The RANSOM registry is considered as a collection of data with the ultimate purpose of gathering information about the effect of renal denervation in patients of the investigator's center and evaluating the results within the usual clinical practice. The general objective of the study is to evaluate the clinical results (blood pressure, quality of life and levels of catecholamines) as well as safety of renal sympathetic denervation in hypertensive patients, at least in treatment with an antihypertensive drug and with increased variability, considering as such a standard deviation> 10 mmHg for systolic BP and> 5 for diastolic BP of its blood pressure levels, measured by ABPM.