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NCT ID: NCT02204891 Completed - Clinical trials for Irritable Bowel Syndrome

Probiotics in Intestinal Bacterial Overgrowth

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of the present study is to demonstrate the effect of a mixture of four species of probiotics (Saccharomyces boulardii, Bifidobacterium lactis BB-12, Lactobacillus acidophilus LA-5 and Lactobacillus plantarum) in patients with symptomatic irritable bowel syndrome (IBS) who have culture verified syndrome of intestinal bacterial overgrowth (SIBO) and those who do not have. This will provide direct evidence for the role of probiotics in treating part of the pathogenesis of IBS.

NCT ID: NCT02198651 Completed - Clinical trials for Rheumatoid Arthritis

A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imaging TEchniques, Drug Levels and Patient Characteristics on the Outcome of Dose TaperIng of Adalimumab in Clinical Remission Rheumatoid ArThritis (RA) Subjects

PREDICTRA
Start date: January 5, 2015
Phase: Phase 4
Study type: Interventional

The primary objective of the study was to investigate the association between residual disease activity at Baseline as detected by Magnetic Resonance Imaging (MRI) and the occurrence of flares in participants with rheumatoid arthritis (RA) randomized to an adalimumab dose tapering regimen controlled by adalimumab withdrawal.

NCT ID: NCT02191150 Completed - Anaemia Clinical Trials

Study of Haemodialysis Patients Switching From Aranesp to Biosimilar

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

The study will obtain data to show insight into clinical outcomes of patients switching from Darbepoetin Alfa to a epoetin alfa biosimilar.

NCT ID: NCT02190175 Completed - Atrial Fibrillation Clinical Trials

Management of Atrial Fibrillation With Flecainide : the AFFLEC Study

Start date: June 2014
Phase:
Study type: Observational

This is a multicentre non interventional observational study with the objective to follow up patients with atrial fibrillation who based on current indications are treated with per os flecainide , for cardiac pulse maintenance.

NCT ID: NCT02185924 Completed - Clinical trials for POSTOPERATIVE ANALGESIA FOR TKA PARECOXIB/CFB

Combination of Continuous Femoral Block and Intravenous Parecoxib For Postoperative Analgesia After Total Knee Arthroplasty

Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Combination of continuous femoral block with parEcoxib vs placebo. Investigation of morphine consumption, opioid sparing effects, VAS pain scores, haemodynamics, Anxierty scores, transfusion requirements , Range of motion and rehabilitation parameters between two groups

NCT ID: NCT02185911 Completed - Anaemia Clinical Trials

Observational Study of Correction of Anaemia With Darbepoetin Alfa at QM Dosing Interval in Patients With CKD Not on Dialysis

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

To describe anaemia correction via haemoglobin measurements taken throughout observation period in ESA naive patients with chronic kidney disease initiated on darbepoetin alfa QM

NCT ID: NCT02184416 Completed - Clinical trials for Metastatic Renal Cell Carcinoma (mRCC)

Study Of The Impact Of Inlyta In 2nd Line On The Treatment Outcomes Of mRCC Patients Treated With Sutent In 1st Line In The Real Life Setting

ADONIS
Start date: October 31, 2014
Phase:
Study type: Observational

This is an international, multi-centre, prospective (partly retrospective), observational study to evaluate treatment patterns and clinical outcomes in patients with advanced or metastatic RCC treated with sunitinib in first line and/or receiving axitinib in second line post sunitinib. The study is designed to enroll approximately 750 patients over the course of an enrollment period of approximately 36 months.

NCT ID: NCT02182752 Completed - Clinical trials for Shoulder Dislocation

The Effect of Tramadol on Interscalene Brachial Plexus Block

Start date: April 2013
Phase: Phase 2
Study type: Interventional

The purpose of our study is to evaluate the effect of tramadol as an adjunct to ropivacaine local anesthetic solution in interscalene brachial plexus block for shoulder surgery.

NCT ID: NCT02181452 Completed - Liver Fibrosis Clinical Trials

Liver Fibrosis Assessment With ShearWave Elastography

Start date: November 2013
Phase: N/A
Study type: Observational

Chronic liver disease/fibrosis can be the result of various causes, and the result is that the liver tissue becomes stiff. ShearWave™ elastography, available on the Aixplorer® ultrasound system, is a method that can be used to measure the stiffness of organs in the body, for example the liver. This study will evaluate how this technology performs as a non-invasive test to stage liver fibrosis in patients with chronic liver disease.

NCT ID: NCT02178475 Completed - Clinical trials for Chemotherapy-induced Febrile Neutropenia

Prospective Observational Study of Febrile Neutropenia (FN) and Pegfilgrastim Primary Prophylaxis in Breast Cancer and Non-Hodgkin's Lymphoma Patients Receiving High (>20%) FN-risk Chemotherapy

Start date: July 18, 2014
Phase:
Study type: Observational

To estimate the incidence of febrile neutropenia in patients with breast cancer and non-Hodgkin's lymphoma receiving high (> 20%) FN-risk chemotherapy and pegfilgrastim primary prophylaxis.