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NCT ID: NCT02774460 Completed - Hypertension Clinical Trials

The Precision Hypertension Care Study

PHYSIC
Start date: February 20, 2017
Phase: Phase 4
Study type: Interventional

The PHYSIC study aims to investigate the potential for precision medicine in the treatment of high blood pressure. It is a double-blind, randomized, repeated cross-over trial with six treatment periods: four classes of blood pressure-lowering drugs where treatment with two classes are repeated for each patient. The classes of blood pressure-lowering drugs to be tested are a diuretic, a calcium channel blocker, an ACE-inhibitor and an angiotensin receptor blocker.

NCT ID: NCT02774447 Completed - Clinical trials for Ileostomy Closure in Rectal Cancer

Day-Case Closure of Loop Ileostomy in Rectal Cancer

Start date: August 2015
Phase:
Study type: Observational

The aim of this study is to investigate if day-case closure of ileostomy is feasible and safe.

NCT ID: NCT02773914 Completed - Dependency Clinical Trials

Comprehensive Geriatric Assessment for Frail Older People

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

The present study "Comprehensive Geriatric Assessment for frail older people in Swedish acute care settings - a randomized controlled study" comprises two study arms: one intervention and one control group. It is a multicentre trial with 5 centres with diverse local conditions in different parts of Sweden, with an implementation study alongside. The intervention "Comprehensive Geriatric Assessment (CGA) for frail older people" addresses people 75 years and older who are seeking acute hospital care at the hospital emergency department, and who are identified as frail. The CGA intervention, including a multidisciplinary team that assesses the patients socio-demographic background, social network, health and medical history, medications, functional status, cognitive status, nutritional status, somatic status and psychosocial status including depression, as well as treatment and planning for discharge and follow-up, contributes to a person-centred, and a comprehensive assessment tailored for each person. The results of this study are expected to optimize the implementation of future complex interventions and lead to the improvement of the care, support and rehabilitation for frail older people with complex needs. This study will contribute to an evidence base for full scale implementation of CGA in Swedish hospital care. The process evaluation, aiming to provide insight into function and consequences of the intervention, why it works or fails, is an important part of the design that will contribute with insights into real life conditions that may be challenging in implementing CGA. The investigators will evaluate fidelity and quality of the implementation, clarify causal mechanisms and identify contextual factors associated with variation in outcomes. The development of screening for frailty and CGA are potential and important tools to identify needs of this older population, and to direct the right health care actions towards those in most need. The study will address the following research questions: 1. Can Comprehensive Geriatric Assessment for frail older patients in Swedish acute hospital settings: - increase/maintain independence, functional status, health related quality of life and life satisfaction? - increase satisfaction with health care? - reduce health care consumption? 2. How feasible and acceptable are the study processes and procedures of CGA from the perspective of care givers and older persons in Swedish settings?

NCT ID: NCT02773641 Completed - Vulvodynia Clinical Trials

Placebo-controlled RCT of Botulinum Toxin A as a Treatment for Provoked Vestibulodynia

Start date: May 2016
Phase: Phase 3
Study type: Interventional

Women with provoked vestibulodynia (PVD) suffer from severe dyspareunia and often present a hyperactivity of the pelvic floor muscles (PFM) which maintain the dyspareunia. The rationale for the study is that for women with PVD who don't succeed to restore the function of the PFM by physiotherapy, Botulinum Toxin A (BTA) could be an optional treatment by decreasing the high muscle tonus and thus possibly reduce the coital pain.

NCT ID: NCT02771054 Completed - HIV Clinical Trials

Tenofovir Alafenamide Fumarate (TAF) Effect on Residual Intrathecal Immune Activation

Start date: May 2, 2016
Phase: Phase 4
Study type: Interventional

Many HIV-infected individuals on effective antiretroviral therapy with suppressed HIV RNA levels in blood as well as in cerebrospinal fluid have signs of low-level intrathecal inflammation. Our aim is to study if changing the nucleoside backbone in an antiretroviral regimen can decrease the residual intrathecal immune activation.

NCT ID: NCT02770846 Completed - Clinical trials for Immediate Dental Implant Loading

Immediate Loading Versus Delayed Loading in Single-implant

Start date: April 2011
Phase: N/A
Study type: Interventional

The purpose of this prospective randomized clinical study was to compare implant survival, patient satisfaction, and radiographic, clinical, and aesthetic outcomes following immediate loading (IL) and delayed loading (DL) of single dental implants after 1,3 and 5 years of follow-up.

NCT ID: NCT02770131 Completed - Clinical trials for Hypercholesterolaemia

Chart Review of Repatha® in Subjects With Hyperlipidaemia

HEYMANS
Start date: May 4, 2016
Phase:
Study type: Observational

Review of clinical characteristics of patients who are prescribed Repatha® and how their treatment is managed.

NCT ID: NCT02767180 Completed - Clinical trials for Intensive Care Unit Syndrome

Evaluation of an ICU-specific Questionnaire for Patient-reported Outcome Measures

Start date: April 2016
Phase:
Study type: Observational

An ICU-specific questionnaire for patient reported outcome measures (PROM) after critical care will be tested in a study of 650 patients recruited six months to three years after discharge from the ICU, and 150 controls who have not been critically ill, matched for age and sex. The questionnaire is sent by mail after an invitation letter followed by a phone call and returned in a pre-stamped envelope. It is then scanned and data imported digitally. Medical data from the ICU-stay can be added. Further analyses after comparison with the control population and item reduction will follow.

NCT ID: NCT02767154 Completed - Heart Disease Clinical Trials

Dextran-based Priming vs. Crystalloid and Mannitol-based Priming Solution in Adult Cardiac Surgery

Start date: May 2016
Phase: Phase 2
Study type: Interventional

This study will compare two priming solutions for extracorporeal circulation, one based on Dextran 40, one based on crystalloid and mannitol. Primary endpoint is oncotic pressure during cardiopulmonary bypass. Secondary endpoints included fluid balance and organ functions.

NCT ID: NCT02765204 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Single-dose Cross-over Study to Assess Direct and Indirect Effects of Dapagliflozin on Pancreatic Alpha and Beta Cells in Patients With Type 2 Diabetes

Start date: March 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate if Dapagliflozin has direct effect on alpha cell glucagon release.