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NCT ID: NCT02481284 Completed - Clinical trials for Breast Reconstruction

Microcirculation of the Abdominal Skin After Deep Inferior Epigastric Artery Perforator Flap Procedure

Start date: January 2008
Phase: N/A
Study type: Observational

The purpose of this study was to perform a quantitative perfusion study of the undermined abdominal skin in deep inferior epigastric artery perforator flap breast reconstruction patients in order to obtain more knowledge on perfusion dynamics. Laser Doppler perfusion imaging (LDPI) was used to evaluate this. Microcirculatory changes were monitored in the abdominal skin of 20 consecutive patients. Measurements were taken and recorded within four standardized zones covering the skin between the xiphoid process and the upper incisional boundary of the flap (zone 1-4; cranial to caudal).

NCT ID: NCT02481011 Completed - Stroke Clinical Trials

Risk of Intracranial Hemorrhage in Users of Oral Antithrombotic Drugs

RICH
Start date: May 2015
Phase:
Study type: Observational

The true incidence and risks of intracranial hemorrhage (ICH) in patients on various antithrombotic treatments remain unknown. Here a nationwide study is conducted to investigate the risk for and incidence rates of ICH in users and non-users of various oral antithrombotic drugs in Norway between 2008 through 2014. Hopefully, this study will contribute to a more responsible prescription pattern of antithrombotic medications.

NCT ID: NCT02480504 Completed - Obesity Clinical Trials

Effects of a 5:2 Diet on Weight Loss and Cardiovascular Risk Factors in Obesity

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

A randomized clinical trial comparing the effect on weight reduction and cardiometabolic risk factors of intermittent energy restriction and a isocaloric continuous energy restriction in obese subjects.

NCT ID: NCT02479841 Completed - Quality of Life Clinical Trials

Health-promoting Competence, Coping and Quality of Life in Patients With COPD

REKV-13/1741
Start date: February 2015
Phase: N/A
Study type: Interventional

Chronic obstructive pulmonary disease (COPD) is a major cause of mortality and disability, and by 2020, it is expected to be the third leading cause of mortality worldwide. COPD is a major public health concern and has considerable impact on health and quality of life. For this study an evidence based self-management program is developed, the purpose of the study is to see if this self-management program, in collaboration between specialized health services and municipality health services, improves patients with COPD health-promoting competence, coping and quality of life, and reduces health service costs.The study has a RCT design.

NCT ID: NCT02479152 Completed - Cardiac Arrest Clinical Trials

The Haemodynamic Effects of Mechanical Standard and Active Chest Compression-decompression During Out-of-hospital CPR

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

The aim of this randomized out-of-hospital cardiopulmonary resuscitation study is to investigate haemodynamics generated by the standard mechanical external chest compression device (LUCAS™ 2) compared to a new version generating chest compressions and active decompression above the initial starting position of the suction cup (LUCAS™ 2AD).

NCT ID: NCT02478502 Terminated - Testicular Cancer Clinical Trials

Testis CAB: Cabazitaxel as Salvage Treatment for Cisplatin-resistant Germ Cell Cancer

Start date: June 2015
Phase: Phase 2
Study type: Interventional

Germ cell tumors belong to the most chemosensitive malignancies. Paclitaxel in combination with ifosfamide and cisplatin (TIP) has become a common regimen for salvage treatment of germ cell cancer. Cabazitaxel may overcome resistance to docetaxel and paclitaxel and might have clinical activity in patients with metastatic and progressive germ cell tumors.

NCT ID: NCT02476461 Recruiting - Clinical trials for Dupuytrens Contracture

Prospective Randomized Trial Between Needle Fasciotomy and Xiapex for Dupuytrens Contracture

PNFvsxiapex
Start date: April 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate whether percutaneous needle fasciotomy is as effective for treating Dupuytrens contracture as Xiapex. Immidiate treatment effect is to be investigated, as iskontracture size after 5 years. Contracture size after one and three years, and subjective hand function is also to be investigated.

NCT ID: NCT02475187 Terminated - Thromboembolism Clinical Trials

Observational Study of Thrombogenic Properties in 220 Patients With Proximal Femur Fracture

thro-fract15
Start date: September 2015
Phase:
Study type: Observational

Measurement of thrombogenic properties by TEG and MEA and observation of thrombotic events over 2 years in 220 patients with hip fracture.

NCT ID: NCT02472535 Completed - Clinical trials for Homozygous Familial Hypercholesterolemia

Study to Evaluate the Effects of MBX-8025 in Patients With HoFH

Start date: April 2015
Phase: Phase 2
Study type: Interventional

A 12-week, open-label, dose-escalating, phase 2 study to evaluate the effects of MBX-8025 in patients with Homozygous Familial Hypercholesterolemia (HoFH).

NCT ID: NCT02471560 Completed - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

Tecfidera and the Gut Microbiota

TECONGUT
Start date: November 6, 2015
Phase: Phase 4
Study type: Interventional

The primary objective of the study is to determine if dimethyl fumarate (DMF) causes changes in the abundance and diversity of commensal microbiota. The secondary objectives of this study are as follows: To identify if there are differences in the gut microbiota composition between patients that do or do not develop gastro intestinal (GI) adverse events (AEs), both pre- and post DMF treatment and to examine if the resolution of GI AEs in DMF treated patients is reflected in the gut microbiota.