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NCT ID: NCT03433729 Completed - Clinical trials for Respiratory Tract Diseases

Patient Agenda Setting and Clinic Efficiency in Outpatients

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

The purpose of the study is to determine whether patients who use a prompt sheet to identify their important issues before they see a doctor are more likely to feel that their important issues have been discussed during their consultation. The study will be conducted in a respiratory outpatient clinic.

NCT ID: NCT03433573 Completed - Diabetes Mellitus Clinical Trials

Paediatric Use of the Abbott Sensor Based Glucose Monitoring System

PUGS
Start date: February 16, 2018
Phase: N/A
Study type: Interventional

Accuracy evaluation of the Abbott Sensor Based Glucose Monitoring System when used by children with diabetes.

NCT ID: NCT03433118 Completed - Cancer Clinical Trials

Acupuncture in Cancer Patients Undergoing Radiotherapy Treatment

ART
Start date: August 12, 2015
Phase: N/A
Study type: Interventional

Feasibility randomized controlled trial of standard care v standard care + acupuncture administered by specially-trained therapy radiographers in patients undergoing radiotherapy. It is a feasibility study to investigate all aspects of a future definitive randomized controlled trial, including statistical power calculation, hence there is no primary outcome or time point. Mixed methods: literature review, model validity, training and mentoring of radiographers, processes, resources, interventions, procedures, patient clinical outcomes, patient and stakeholder qualitative outcomes

NCT ID: NCT03432962 Completed - Diet Surveys Clinical Trials

Brand Level Nutrient Information Compared to Generic Food Codes

Start date: October 1, 2015
Phase: N/A
Study type: Observational

Measuring diet is difficult. This is the first time that brand level foods and nutrient values have been compared with generic food codes to explore the difference this might make to estimated nutrient intakes.

NCT ID: NCT03432871 Completed - Clinical trials for Mitochondrial Diseases

Nicotinamide Riboside and Mitochondrial Biogenesis

Start date: December 8, 2017
Phase: N/A
Study type: Interventional

Mitochondria are important parts of the cell that are responsible for producing energy. The amount of energy they produce depends on how much energy the body needs to function and this energy production can be severely impaired in people with mitochondrial disease. Symptoms of mitochondrial disease vary widely but usually involve the brain, nerves and muscles, as these are tissues that need a lot of energy. Mitochondrial disorders affect 1 in 5000 of the UK population and there is currently no cure. Some scientists think that increasing the number of mitochondria in the body (mitochondrial biogenesis) might be an effective treatment for the symptoms of mitochondrial disease. Studies carried out in mice have shown that a type of B-vitamin called Nicotinamide Riboside (NR) is able to increase the number of mitochondria, leading to increased energy and a reduction in the symptoms of mitochondrial disease. The aim of this study is to investigate if the same B vitamin, Nicotinamide Riboside, can increase energy production and reduce symptoms in humans with mitochondrial disease. The study will consist of two parts: Part 1: Participants will be given a single oral dose of Nicotinamide Riboside and the levels of NR in their bloodstream will be measured at regular intervals. This will involve a single overnight stay and simple blood tests. Part 2: This requires 6 separate visits from each participant. Each participant will undergo a series of standard tests including a muscle biopsy and an MRI scan, then they will take a course of Nicotinamide Riboside (twice daily for 4 weeks). After 4 weeks of treatment, the participants will undergo the same tests again to see if there have been any changes in response to the treatment.

NCT ID: NCT03432533 Completed - Clinical trials for Post-Menopausal Osteoporosis

A Comparison of Subject-administered Romosozumab With Healthcare Provider-administered Romosozumab for Osteoporosis

Start date: February 6, 2018
Phase: Phase 3
Study type: Interventional

To evaluate the noninferiority of a 6-month treatment with 210 mg romosozumab at 90 mg/mL administered subcutaneously (SC) once a month (QM) in postmenopausal women with osteoporosis either by healthcare provider (HCP) administration with prefilled syringe (PFS) or by subject self-administration with autoinjector/pen (AI/Pen)

NCT ID: NCT03432429 Completed - Breast Cancer Clinical Trials

Real Time Tissue Characterisation Using Mass Spectrometry REI-EXCISE iKnife Study

REI-EXCISE
Start date: September 5, 2017
Phase:
Study type: Observational

REI-EXCISE is a multicentre, prospective, non-randomised feasibility study, aimed to evaluate the diagnostic accuracy of rapid ionisation mass spectroscopy using an iKnife device. The iKnife will collect vapour, a by-product of surgery, which will pass through the mass spectrometer machine for analysis in order to evaluate what is "normal" and what is "cancerous" breast tissue.

NCT ID: NCT03431662 Completed - Osteoarthritis Clinical Trials

Computerized Tomography (CT) Scan Study of Bone Healing Following Open Wedge Proximal Tibial Osteotomy

CISKO
Start date: March 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess whether there is a difference between the TomoFix and Ellipse Intramedullary HTO Nail System in terms of bone regeneration in the tibial wedge by performing a CT-scan at 3 and 6-months postoperatively.

NCT ID: NCT03430843 Completed - Clinical trials for Esophageal Squamous Cell Carcinoma (ESCC)

A Study of Tislelizumab (BGB-A317) Versus Chemotherapy as Second Line Treatment in Participants With Advanced Esophageal Squamous Cell Carcinoma

Start date: January 26, 2018
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the efficacy and safety of tislelizumab as second line treatment in participants with advanced unresectable/metastatic ESCC that had progressed during or after first line therapy.

NCT ID: NCT03430219 Completed - Bone Marrow Edema Clinical Trials

Subchondroplasty Procedure in Patients With Bone Marrow Lesions

Start date: March 1, 2018
Phase:
Study type: Observational

This is a prospective, multi-center, post-market data collection study intended to collect data on the short- and long-term safety and performance of the SCP Procedure.