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Morbidity clinical trials

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NCT ID: NCT03245658 Withdrawn - Mortality Clinical Trials

The Effect of Cannabis in Pancreatic Cancer

Start date: October 6, 2017
Phase: Phase 2
Study type: Interventional

Cannabinoids are known to increase appetite, but THC components have psychogenic properties too. CBD is the main component in the plant, and have only minimal psychogenic effects. The aim was to test the appetite stimulating effects of CBD in patients with pancreatic cancer in palliative treatment.

NCT ID: NCT02845726 Completed - Morbidity Clinical Trials

Biofilms on Short-term Indwelling Ureteral Stents

Start date: July 2016
Phase: N/A
Study type: Observational

This study is performed to analyze various aspects of biofilms on ureteral stents.

NCT ID: NCT02448615 Completed - Child Development Clinical Trials

Birth Cohort in Coast Province, Kenya

Start date: July 2015
Phase: N/A
Study type: Observational

In 2010, 7.6 million children under the age of five died worldwide and yet the causes of only 2.7% (0.205 million) of these deaths were medically certified. A thorough understanding of the causes of child mortality is necessary to guide research efforts aimed at tackling this important global health problem. Prospective birth cohort studies present an opportunity to examine the relationships between early-life exposures and multiple health and non-health related outcomes including death, illness, and socioeconomic factors. In this study, the investigators will provide insight into the underlying causes of child mortality by collecting data on early-life exposures and health and non-health related outcomes in the first year of life.

NCT ID: NCT02447536 Completed - Morbidity Clinical Trials

Trial of Two Strains of BCG

BCGSTRAIN
Start date: December 8, 2014
Phase: Phase 4
Study type: Interventional

The investigators aim to conduct a randomised controlled trial comparing two Bacille Calmette-Guérin (BCG) strains currently used in Guinea-Bissau, the Danish and the Russian, in terms of prevention of neonatal and early life morbidity and mortality, immune responses and adverse events related to BCG vaccination. The primary outcome will be hospital admissions within 6 weeks of age.

NCT ID: NCT02121886 Recruiting - Safety Clinical Trials

The Parietal Peritoneum as a Substitute Graft for Venous Reconstruction in HPB Surgery

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

To evaluate the safety and outcome of the parietal peritoneum for venous reconstruction HPB surgery. Although the parietal peritoneum had already been used and published for the reconstruction of the vena cava, however this one was never described or described in HPB surgery

NCT ID: NCT02118545 Completed - Mortality Clinical Trials

Von Willebrand Factor to Predict Postoperative Outcome

Start date: April 2014
Phase: N/A
Study type: Observational

vWF is stored in weibel-palade-bodies of endothelial cells as well as alpha-granula of platelets and is released upon their activation. Endothelial cell dysfunction as well as platelet activation often occur in liver disease and portal hypertension, which may lead to an increase in circulating vWF levels. Indeed, multiple studies have reported that liver disease is associated with increased circulating vWF- antigen (vWF-Ag). Furthermore, increased circulating vWF -Ag Levels have been shown to be associated with increased mortality rates in patients with chronic liver disease. Within a prospective evaluation cohort, the investigators were able to document that patients with increased vWF-Ag levels prior to liver resection suffered from an increased incidence of postoperative liver dysfunction and morbidity. Within this prospective multicenter validation study, the investigators now aim to prospectively validate that circulating vWF-Ag prior to liver resection is a valuable marker to predict postoperative clinical outcome.

NCT ID: NCT01883193 Completed - Mortality Clinical Trials

Women First: Preconception Maternal Nutrition

WF
Start date: August 2013
Phase: N/A
Study type: Interventional

Multi-country three-arm, individually randomized, non-masked, controlled trial to ascertain the benefits of ensuring optimal maternal nutrition before conception and providing an evidence base for programmatic priority directed to minimizing the risk of malnutrition in all females of reproductive age.

NCT ID: NCT01631799 Completed - Mortality Clinical Trials

Outcome of Patients After Total Knee Replacement: A Comparison of Femoral Nerve Block and Epidural Anesthesia

Start date: October 2008
Phase: N/A
Study type: Interventional

Total knee replacement is very common in Germany. After surgery patients have severe pain in the knee; initiation of the physiotherapy, however, is important in the first three days after surgery. Continuous femoral blockade and continuous (lumbar) epidural analgesia are commonly used after surgery. Both methods are used in Germany. Both methods have advantages and disadvantages. We wanted to answer the question which method of analgesia - after total knee replacement - is better concerning complications and function (after 3 months) ?

NCT ID: NCT01396993 Active, not recruiting - Quality of Life Clinical Trials

Prospective Non-randomized Evaluation of Oncoplastic Surgery

iTOP
Start date: July 2011
Phase: N/A
Study type: Observational

Breast conserving therapy (BCT) is the standard treatment for intraductal or invasive breast cancer patients. However cosmetic results, e.g. symmetry and nipple displacement, are sometimes poor reducing the quality of life. The use of immediate techniques for oncoplastic surgery (iTOP) seems to improve subjective cosmetic outcome. Oncologic safety of iTOP has been demonstrated by several authors using restrospective analyses. However, no prospective observational trial has been done to objectively evaluate cosmetic and oncologic outcome comparing BCT with iTOP. The aim of this study is to investigate this issue within a prospective non randomized observational trial at the Medical University Vienna.

NCT ID: NCT01069107 Completed - Morbidity Clinical Trials

Acute Admission to Hallingdal Sjukestugu

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

The main objective of the project is to assess whether a community hospital may have or should have a role in the Norwegian health care system in the acute treatment of a defined group of patients.