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NCT ID: NCT02175875 Completed - Comatose Clinical Trials

Ticagrelor for the Comatose

TICOMA
Start date: September 2014
Phase: N/A
Study type: Observational

The study will investigate the effect of the oral antiplatelet agent ticagrelor (Brilique) when it is administrated through a nasogastric tube in comatose patients. The platelet function can be determined by various platelet function tests (PFT), Multiplate and VerifyNow . As control, the reference intervals from the literature are used. Futhermore, plasma concentrations of the active metabolite will be determined at aeveral timepoints after first intake of a bolus dose.

NCT ID: NCT02175862 Completed - Wounds and Injuries Clinical Trials

Long-term Evaluation of Patients Treated by an Emergency Medical Helicopter

Start date: December 2009
Phase: N/A
Study type: Observational [Patient Registry]

In May 2010 the first danish physician-staffed Helicopter Emergency Medical Service (PS-HEMS) was implemented in Region Zealand and the Capital Region (excluding Bornholm) of Denmark. In relation to the introduction of PS-HEMS, a team of collaborators lead by Rasmus Hesselfeldt, conducted an observational study to investigate the possible effects on time to definitive care, secondary transfers and 30-day mortality in a "before" and "after" design. Results showed reduced time from first dispatch to arrival at the trauma centre from 218 min to 90 min. Secondary transfers to the trauma centre dropped from 50 % to 34 % and 30-day mortality significantly reduced from 29 % to 14 % in the year after implementation. The present study is an observational cohort study with long-term follow-up of the same trauma population as mentioned above. Patients were followed until may 1st, 2014. Primary outcome is early retirement and secondary outcomes are quality of life and mortality. The investigators hypothesize that a greater proportion of trauma patients in the "after" period will remain in occupation after approx. 3 to 4.5 years compared with trauma patients treated in the "before" period.

NCT ID: NCT02174861 Completed - Clinical trials for Treatment for Prevention of Chronic Migraine

A Study to Assess the Long-term Safety and Efficacy of Erenumab (AMG 334) in Chronic Migraine Prevention.

Start date: June 30, 2014
Phase: Phase 2
Study type: Interventional

To assess the long-term safety and efficacy of erenumab.

NCT ID: NCT02174666 Completed - Osteoporosis Clinical Trials

Isoflavone Treatment for Postmenopausal Osteopenia.

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

The aim of the project is to execute a double-blind, parallel, randomized 12-month intervention trial on postmenopausal women with osteopenia (low bone mineral density), in order to determine the effects of daily intake of fermented red clover (RC) extract on estrogen dependent bone mineral resorption when compared to placebo. Both groups will recieve equivalent daily calcium, vitamin D and magnesium supplements. The project will also assess whether bioactive compounds in RC can reduce the risk of developing cardiovascular disease.

NCT ID: NCT02173483 Completed - Clinical trials for Rupture of Anterior Cruciate Ligament

Anterior Cruciate Ligament-reconstruction: Quadriceps Tendon or Hamstrings Tendon? A Prospective Trial

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

The purpose of this study is to determine whether there is a difference in muscle strength after anterior cruciate ligament comparing 2 surgery technics. Using either autograft hamstrings tendon or a autograft quadriceps tendon.

NCT ID: NCT02173418 Completed - Postoperative Pain Clinical Trials

The Effect of Phrenic Nerve Blockade on Acute and Chronic Shoulder Pain in Patients for Lobectomy and Pneumonectomy

TOPBLOC
Start date: November 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study was to test whether peroperative infiltration of the phrenic nerve during lung surgery would protect patients against postoperative shoulder pain.

NCT ID: NCT02172729 Completed - Healthy Clinical Trials

The Effect of Different Doses (Mass) of Local Anesthetic on Duration of Adductor Canal Block in Healthy Volunteers - Part 2

Start date: June 2014
Phase: Phase 4
Study type: Interventional

To investigate whether increased dose of local anesthetic (lidocaine) increases duration of peripheral nerve block (adductor canal block) and to develop a model for assessing duration of peripheral nerve blockades. The investigators hypothesize that increasing the dose of lidocaine (by increased concentration) will increase the duration of an adductor canal block. The study is a follow up on an identical study (SM1-PJ-13, EudraCT number: 2013-001822-24 ) made earlier with different concentrations of lidocaine and a placebo group. For further information see trial registration at European Union Drug Regulatory Authorities Clinical Trial System.

NCT ID: NCT02170428 Completed - Clinical trials for Overweight or Obesity

Diet and Well-being of Young Danish Children

SKOT I
Start date: May 2007
Phase:
Study type: Observational

The overall objective with the study was to contribute to the scientific basis for dietary and life strategies, policies and dietary guidelines to infants and young children in Denmark and with special focus on prevention of obesity and diet related chronic diseases such as type 2 diabetes, ischemic heart disease and osteoporosis.

NCT ID: NCT02169011 Completed - Clinical trials for Breast Reconstruction

Secondary Breast Reconstruction With a Flap of Skin From the Back

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the different outcomes of breast reconstruction in women who are treated for breast cancer with mastectomy and subsequently have delayed breast reconstruction by one of two different surgical techniques both of which are based on the use of a tissue flap from the patient's back. These techniques are either a latissimus dorsi flap (LD-flap) or a thoracodorsal artery perforator flap (TAP-flap) The main objective of the study is to establish whether one of these techniques may result in a superior outcome and thus should be recommended as first choice treatment rather than the other.

NCT ID: NCT02167087 Completed - Colon Cancer Clinical Trials

Sentinel Node Mapping With Indocyanine Green in Colon Cancer: a Feasibility Trial and a Descriptive Serie.

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

This study is a clinical feasibility trial that will contribute to the clarification of whether sentinel node mapping with indocyanine green (ICG) provides a better basis for staging of colorectal cancer.