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NCT ID: NCT02299544 Completed - Over Active Bladder Clinical Trials

BlueWind Medical System for the Treatment of Patients With OAB

OAB
Start date: February 2015
Phase: N/A
Study type: Interventional

BlueWind system safety and performance in treatment of patients diagnosed with overactive bladder (OAB)

NCT ID: NCT02299505 Completed - Clinical trials for Non-Small Cell Lung Cancer

Pharmacokinetic and Safety Study of Lower Doses of Ceritinib Taken With a Low-fat Meal Versus 750 mg of Ceritinib in the Fasted State in Adult Patients With (ALK-positive) Metastatic Non-small Cell Lung Cancer (NSCLC)

Start date: April 9, 2015
Phase: Phase 1
Study type: Interventional

A Phase I study to assess the systemic exposure, effiacy, and safety of 450 mg ceritinib taken with a low-fat meal and 600 mg ceritinib taken with a low-fat meal as compared with that of 750 mg ceritinib taken in the fasted state in adult patients with ALK rearranged (ALK-positive) metastatic non-small cell lung cancer (NSCLC)

NCT ID: NCT02299362 Completed - Clinical trials for Thoracic Insufficiency Syndrome

The Treatment of Progressive Early Onset Spinal Deformities: A Multi-Center Outcome Study

GSSG
Start date: October 2008
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to examine the treatment, both surgical and non-surgical, of patients with any form of early onset scoliosis. Such treatment may include the use of growth friendly devices that are surgically or magnetically lengthened; or the use of serial body casting or bracing, or observation. Outcomes examined will be what can be seen physically on the patient and on x-ray, as well as parent perception of how the treatment effects their child with the use of a health-related quality of life (HRQOL) questionnaire.

NCT ID: NCT02298907 Completed - Colorectal Cancer Clinical Trials

CPET in Colorectal Surgery

Start date: June 2010
Phase:
Study type: Observational [Patient Registry]

The present study is a retrospective analysis of prospectively collected clinical data. Anonymized data from patients collected during routine clinical care from 7 major colorectal units in the UK who perform pre-operative cardiopulmonary exercise testing will be pooled at a central location (Aintree University Hospitals, Liverpool) and used to validate the relationship between cardiopulmonary exercise testing (CPET) variables and short term post-operative outcomes after major colorectal surgery. Here the investigators will attempt to validate a study entitled "Cardiopulmonary exercise variables are associated with postoperative morbidity after major colonic surgery - a prospective blinded observational study" previously published by our team in Liverpool .

NCT ID: NCT02298855 Completed - Ovarian Cancer Clinical Trials

Individualised Versus Conventional Medical Follow-up for Women After Primary Treatment for Ovarian Cancer.

Start date: January 2006
Phase: N/A
Study type: Interventional

The purpose of this study in women who have completed primary treatment for ovarian cancer is to investigate the effects of individualised follow-up care delivered by a nurse compared to conventional medical follow-up on quality of life and mood. The investigators aim to determine if the individualised treatment is acceptable to women compared to the conventional treatment.

NCT ID: NCT02298530 Completed - Healthy Clinical Trials

Tea Components, Mental Stress and Blood Pressure

Start date: March 2015
Phase: N/A
Study type: Interventional

Assess the effects of adding theanine to a caffeinated beverage on changes in blood pressure during acute mental stress.

NCT ID: NCT02298049 Completed - Appetite Clinical Trials

An fMRI Study of Satiation in Healthy Volunteers.

Start date: July 2010
Phase: N/A
Study type: Interventional

To our knowledge no study has assessed the effects of a meal on neural responses to food cues and compared this with a condition simulating natural inter-meal hunger levels. This is important, as the existing literature often compares the effect of fasting to satiation, which may not reflect typical appetite processes. Thus, the purpose of this research was to examine the effect of a satiating lunch compared to a normal pre-meal state on blood oxygen level dependent (BOLD) activity in the human brain, as measured using functional magnetic resonance imaging (fMRI).

NCT ID: NCT02298036 Completed - Clinical trials for Frequent Utilisers of Urgent Medical Care Who Have High Health Anxiety

Helping Urgent Care Users Cope With Distress About Physical Complaints

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

To determine the cost and clinical effectiveness of offering 6-10 sessions of remotely delivered cognitive behaviour therapy (CBT) via video calling or over the telephone for health anxiety in repeated utilisers of unscheduled/urgent care versus treatment as usual. To optimise the delivery of CBT for health anxiety delivered remotely by systematically identifying and then acting on barriers and enablers to the intervention through a network of practice.

NCT ID: NCT02297711 Completed - Hernia Clinical Trials

TEP Versus Open Minimal Suture Repair for the Sportsman's Groin

SPORT
Start date: December 3, 2014
Phase: N/A
Study type: Interventional

Sportsman's hernia is defined as a weakness or disruption of the posterior wall of the inguinal canal. Open hernia repair with or without mesh or laparoscopic techniques with mesh have been advocated in the treatment of sportsman's hernia and associated athletic pubalgia. The results of the operative treatment from single centers are reported to be good to excellent in between 70 - 90% of patients with the most promising results reported using an open minimal repair (OMR) technique. There are no randomized trials comparing open versus laparoscopic techniques regarding time for recovery and relief of pain. The aim of this randomized study is to compare the effectiveness of OMR technique in local or spinal anesthesia to endoscopic Total ExtraPeritoneal (TEP) technique in general anesthesia for the treatment of Sportsman´s hernia/athletic pubalgia. The primary endpoint is patient being free from intractable groin pain during sports activity or daily work four weeks after surgery.

NCT ID: NCT02297451 Completed - Clinical trials for Renal Failure, End-Stage

Trial Comparing the Incidence of Steal Syndrome in the Two Types of anTEcubitaL Fossa Arteriovenous fistuLa AVF

STEAL
Start date: February 2011
Phase: N/A
Study type: Interventional

Background: Arteriovenous fistula (AVF) is a form of vascular access for haemodialysis. An AVF is normally created at the level of the wrist, but occasionally it is created in the elbow when there is no suitable vessel in the forearm. The most common type of elbow (antecubital) fistula (AFF) is a brachiocephalic fistula, which carries significantly higher risk of steal syndrome (AVF-associated hand ischaemia) than wrist fistulas. More recently, AFF using proximal radial or ulnar artery as inflow has been described and shown to have a lower rate of Steal syndrome than brachiocephalic fistula. This study aims to investigate the incidence of steal syndrome between AFF using brachial artery and that using the proximal radial/ulnar artery as inflow.