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NCT ID: NCT03134586 Completed - Crohn Disease Clinical Trials

Advanced Non-Invasive Diagnostics in Inflammatory Bowel Disease

ANDI
Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Non-invasive endoscopic procedures (pillcam colon capsule endoscopy, PCCE) and non-ionizing radiological modalities (MR enterocolonography, MREC and ultrasound, US) - offer a sufficiently high diagnostic validity in patients with suspected CD compared to the traditional invasive approach using ileocolonoscopy with biopsies as first line diagnostic modality

NCT ID: NCT03133741 Completed - Clinical trials for Glucose Metabolism Disorders

Inhibition of the Endogenous GIP Response With a GIP Receptor Antagonist

GA-3
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Delinieation of GIP's effects during an oral glucose tolerance test (OGTT) in humans using GIP receptor antagonisation.

NCT ID: NCT03133364 Completed - Quality of Life Clinical Trials

Developing and Testing Delicious and Nutritious for the Old People

Start date: May 17, 2017
Phase: N/A
Study type: Interventional

Meals-on wheels may play a major role in contributing to better nourishment and quality of life in older people, thus delaying costly hospitalisation. Still, dwelling, old adults who receive meals-on-wheels are a population at risk of undernutrition leading to a decreased quality of life. Hypothesis Offering nutritious ELDORADO meals as meals-on-wheels to nursing home residents in 3 months is an effective way to increase quality of life. Aim To improve quality of life and functional abilities in nursing home residents by offering nutritious ELDORADO meals.

NCT ID: NCT03130166 Completed - Colonic Cancer Clinical Trials

INtracorporeal Versus EXtracorporeal Anastomosis in Robotic Right Colectomy

INEXA
Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Right-sided colonic cancer is treated with right-sided colectomy, predominantly performed as minimally invasive surgery with extracorporeal anastomosis (ECA). In recent years a new technique with intracorporeal anastomosis (ICA) has emerged and it is thought that ICA is less invasive and thereby has the potential to improve the postoperative course of right colonic cancer patients. The objective of this study is to compare robotic right colectomy with either ICA or ECA in a randomized controlled setting.

NCT ID: NCT03130049 Completed - Postoperative Pain Clinical Trials

Popliteal Plexus Block for Postoperative Pain After ACL Reconstruction

Start date: September 27, 2017
Phase: N/A
Study type: Interventional

The study aims to investigate the effect of the popliteal plexus block (PPB) on postoperative pain in patients undergoing anterior cruciate ligament (ACL) reconstruction.

NCT ID: NCT03126591 Completed - Soft Tissue Sarcoma Clinical Trials

A Study of Olaratumab (LY3012207) Plus Pembrolizumab in Participants With Advanced or Metastatic Soft Tissue Sarcoma

Start date: July 3, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety of olaratumab plus pembrolizumab in participants with previously treated advanced or metastatic soft tissue sarcoma.

NCT ID: NCT03125954 Completed - Knee Osteoarthritis Clinical Trials

Changes in Physical Inactivity in Patients With Knee Osteoarthritis

Start date: May 8, 2017
Phase:
Study type: Observational

This is an objective cohort study using objective recording of physical activity (accelerometry) during and after the GLAiD intervention to investigate if a sedentary behavior change by participating in an 6-week physiotherapy-led exercise and education program (GLAiD) occurs. The GLAiD intervention is an education and exercise based intervention aiming at decreasing pain and improving function in patients with knee osteoarthritis. The primary outcome is change in objective recorded physical activity between baseline and follow-up.

NCT ID: NCT03125941 Completed - Breast Cancer Clinical Trials

High vs Low Dose Dexamethasone on Complications in the Immediate Postoperative Phase After Mastectomy

DEX-MAS
Start date: March 27, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to investigate the effect of a single preoperative high-dose steroid injection on complications in the immediate postoperative phase after breast cancer surgery, with removal of the breast (mastectomy). Primary outcome is the proportion patients who require transfer to the post anaesthesia care unit (PACU) and the proportion that can be transferred directly to the ward. Secondary outcomes are organospecific complications in the postanesthesia phase, pain and nausea the first 5 days, seroma and wound infection the first 14 days and readmissions the first 30 days after surgery. The investigators hypothesize that the frequency of transfer to the PACU and organospecific complications will be lower among patients receiving high dose dexamethasone. The investigators hypothesize, that there will be no difference in wound infections, seroma or readmissions.

NCT ID: NCT03124511 Completed - Clinical trials for Chronic Chemotherapy-induced Pain

Neuropathic Pain After Breast Surgery

Start date: August 15, 2017
Phase:
Study type: Observational

To understand pain pathophysiology in terms of risk factors and protective mechanisms ranging from molecular pathways to societal impacts.

NCT ID: NCT03123120 Completed - Colitis, Ulcerative Clinical Trials

A Study in Patients With Mild or Moderate Ulcerative Colitis Who Take a TNF Inhibitor. The Study Investigates Whether Bowel Inflammation Improves When Patients Take BI 655130 in Addition to Their Current Therapy

Start date: June 7, 2017
Phase: Phase 2
Study type: Interventional

The objectives of this trial are safety and efficacy (proof-of-concept) of induction of mucosal healing by BI 655130 add-on therapy in patients with mild or moderate ulcerative colitis and persisting endoscopic activity despite pre-existing TNFi treatment. This trial will explore safety and efficacy of a dose of BI 655130 that was modelled to achieve the similar exposures as the highest exposures tested and found safe and tolerable in preceding single and multiple dose studies in healthy subjects, as add-on to pre-existing TNFi (Tumor necrosis factor inhibitor) treatment. Secondary and further objectives include assessment of the pharmacokinetic (PK) profile of BI 655130 and early exploration of specific biomarkers with potential usefulness to predict clinical efficacy or safety outcome or help understand BI 655130's mode of action.