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NCT ID: NCT02440763 Recruiting - Clinical trials for Spinocerebellar Ataxia

The EUROSCA Natural History Study

EUROSCA-NHS
Start date: July 2005
Phase: N/A
Study type: Observational

The key goals of EUROSCA-NHS is to determine and compare the rate of disease progression in SCA1, SCA2, SCA3 and SCA6 including determination of the order and occurrence of non-ataxia symptoms, assessment of activities of daily living (ADL) and quality of life (QoL), and identification of predictors of disease progression and survival.

NCT ID: NCT02417623 Recruiting - Obesity Clinical Trials

Smartphone Application for Weight Loss

OBSBIT
Start date: January 2015
Phase: N/A
Study type: Interventional

AIM: To assess the efficacy of an intervention that includes the assistance of a weight loss smartphone application targeted to young people aged 18 to 40 years. DESIGN: Randomisedclinical trial. SETTING: Primary Health Care centres (PHCCs) in Catalonia. PARTICIPANTS: Adults aged 18 to 40 years with criteria of obesity or overweight, consulting PHCCs for any reason and who provide written informed consent to participate in the trial. INTERVENTION GROUP will receive a 12-month weight loss programme that implements recommendations of a Clinical Practice Guideline, complemented with a smartphone app designed specifically for this programme. CONTROL GROUP will receive the usual care. The outcome measure will be weight loss at 12 months. EXPECTED RESULTS: The investigators expect a higher weight loss in the intervention group than in control group.

NCT ID: NCT02409511 Recruiting - Clinical trials for Diabetic Retinopathy

Microalbuminuria as a Cardiovascular Risk Factor (PRECISED Substudy)

Start date: January 2016
Phase: N/A
Study type: Observational

Microalbuminuria (MA) is an independent cardiovascular risk factor in diabetic and non-diabetic subjects. However, in the setting of type 2 diabetes, microalbuminuria could be a marker of either early diabetic nephropathy or diffuse endothelial dysfunction. At present, there are no biomarkers that permit us to discriminate between these two conditions.

NCT ID: NCT02404987 Recruiting - Malnutrition Clinical Trials

An Oral Nutritional Supplement Study in Older Malnourished Spanish Population

Start date: June 2014
Phase: N/A
Study type: Observational

Post-marketing observational study of a nutritional care plan, including a higher calorie, higher protein oral nutritional supplement (ONS), prescribed to Spanish patients, both free living and residing and nursing homes, who have been identified as malnourished. The objective is to assess the impact of the ONS on body weight, activities of daily living and quality of life.

NCT ID: NCT02401620 Recruiting - Clinical trials for Rheumatoid Arthritis

Validation of a Tolerability Questionnaire in Rheumatoid Arthritis

Start date: January 2014
Phase: N/A
Study type: Observational

The purpose of the present study is to assess the measurement properties of a tolerability questionnaire. The results obtained in patients with Rheumatoid Arthritis (RA) being treated will be robust and will assess the patient's tolerability to the treatment. Patients with greater tolerability will be more satisfied with their treatment.

NCT ID: NCT02401490 Recruiting - Cirrhosis Clinical Trials

Albumin Infusion Effects in Mortality in Patients With Cirrhosis and Hepatic Encephalopathy

BETA
Start date: April 2015
Phase: Phase 4
Study type: Interventional

To assess whether albumin administration after an episode of hepatic encephalopathy (≥ grade II) improves survival at 90 days (mortality endpoint treated as a composite endpoint death and/ or liver transplantation).

NCT ID: NCT02399488 Recruiting - Clinical trials for Sphb Haemoglobin in Vivo Validation

Validation of Continuous Noninvasive Haemoglobin Monitoring by the Radical 7 Pulse CO-Oximetry Monitor After in Vivo Adjustment.

Start date: February 2012
Phase: N/A
Study type: Observational

Continuous haemoglobin determination could improve the outcomes of several patients in risk of bleeding during surgery. An in vivo calibration has been introduced to the device after our team found its need. The uncalilbrated validation of the Masimo Radical 7 continuous haemoglobin monitor has been made in various papers, although it has been compared to point of care devices, thus introducing an error as such point of care devices although validated for haemoglobin determination, are not as accurate as the gold standard. The validation of the gold standard calibrated device has not been described yet. When compared to the accepted gold standard (cyanmethemoglobin method, Coulter), accuracy and precision of the continuous haemoglobin monitor could be good enough to be used interchangeably with the gold standard.

NCT ID: NCT02395419 Recruiting - Clinical trials for Endotracheal Intubation

A Comparison of Tracheal Intubation Using the Totaltrack vs the Airtraq Laryngoscope in Routine Airway Management

Start date: October 2016
Phase: N/A
Study type: Interventional

Endotracheal intubation is usually required to allow unrestricted surgical approach. The Macintosh laryngoscope is the standard method. However in certain situations as difficult airway this technique is ineffective and poorly tolerated by the patient. Fiberoptic intubation is the gold standard in this scenario, however sometimes it is not possible due to failure or unavailability, so alternatives are needed. The TotalTrack (MedComflow SA, Barcelona, Spain) and the Airtraq (Prodol Meditec, Vizcaya, España) been designed specifically for the airway management. However, despite their use in clinical practice, there are no comparative studies.

NCT ID: NCT02395406 Recruiting - Clinical trials for Endotracheal Intubation

A Comparison of Tracheal Intubation Using the Totaltrack vs the Airtraq Laryngoscope in Difficult Airway Management

Start date: October 2016
Phase: N/A
Study type: Interventional

Endotracheal intubation is usually required to allow unrestricted surgical approach. The Macintosh laryngoscope is the standard method. However in certain situations as difficult airway this technique is ineffective and poorly tolerated by the patient. Fiberoptic intubation is the gold standard in this scenario, however sometimes it is not possible due to failure or unavailability, so alternatives are needed. The TotalTrack (MedComflow SA, Barcelona, Spain) and the Airtraq (Prodol Meditec, Vizcaya, España) been designed specifically for the airway management. However, despite their use in clinical practice, there are no comparative studies.

NCT ID: NCT02395354 Recruiting - Crohn's Disease Clinical Trials

Comparative Prospective Multicenter Randomized Study of Endoscopic Treatment of Stenosis in Crohn´s Disease

PROTDILAT
Start date: September 2013
Phase: N/A
Study type: Interventional

This study will be a multicentre randomized controlled trial to assess the efficacy between balloon dilatation and self-expanding metallic stent placement for endoscopic treatment of stenosis in Crohn´s Disease.