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NCT ID: NCT00939003 Completed - Clinical trials for Axial Spondyloarthritis

Study of Adalimumab in Patients With Axial Spondyloarthritis

Start date: July 2009
Phase: Phase 3
Study type: Interventional

This study will evaluate how well adalimumab works in the short and long term in patients with axial spondyloarthritis who are not diagnosed as having either ankylosing spondylitis or psoriatic arthritis.

NCT ID: NCT00938730 Completed - Atrial Fibrillation Clinical Trials

A Study Evaluating Safety and Tolerability of YM150 Compared to Warfarin in Subjects With Atrial Fibrillation

OPAL-2
Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the optimal daily dose and dose regimen of YM150 in subjects with non-valvular atrial fibrillation (NVAF), primarily based on safety and tolerability data.

NCT ID: NCT00938639 Completed - Clinical trials for Influenza Caused by the Novel Influenza A (H1N1) Virus

A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in Healthy Adults

Start date: July 2009
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether CSL425 is a safe and effective vaccine for eliciting an immune response to H1N1 influenza in healthy adults.

NCT ID: NCT00937950 Completed - Clinical trials for Infections, Papillomavirus

Gynaecological Follow-up of a Subset of 580299/008 (NCT00122681) Study Subjects

Start date: August 5, 2009
Phase: Phase 3
Study type: Interventional

This study is designed to provide up to four years of annual oncogenic HPV DNA testing and cervical cytology examination for NCT00122681 study subjects who displayed normal cervical cytology but tested positive for oncogenic HPV infection at their last NCT00122681 study visit (Visit 10, Month 48). This follow-up study will also be offered to subjects who were pregnant at their last NCT00122681 study visit (Visit 10, Month 48) so that no cervical sample could be collected at that visit. The objectives & outcome measures of the primary phase (study 008/580299) are presented in a separate protocol posting (NCT00122681).

NCT ID: NCT00936312 Completed - Hemophilia A Clinical Trials

Females With Severe or Moderate Hemophilia A or B: an International Multi-center Study

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

This is a multi-center, international study designed to collect clinical, genetic and quality of life information on females with hemophilia, an inherited bleeding disorder. The study is designed to determine whether there are problems and issues unique to females with hemophilia.

NCT ID: NCT00936078 Completed - Clinical trials for Living Kidney Donation

The Living Kidney Donor Safety Study

LKD
Start date: September 2009
Phase:
Study type: Observational

The main goal of this study is to understand the long-term effects of kidney donation on blood pressure, kidney function, and patient-reported health-related quality of life. Living kidney donors and non-donor controls will be studied before and after the living donor transplant. The donors and non-donors will be followed for a minimum of 5 years and a maximum of 15 years. Both groups will be made up of healthy normotensive adults. The purpose of this study is to see if there are any long-term differences between the two groups regarding: 1. risk of hypertension 2. rate of kidney decline 3. risk of albuminuria 4. changes in health-related quality of life The study also looks to assess other outcomes, including: 1. understand and quantify the expenses incurred by donors 2. understand donor factors which influence recipient outcomes The pilot version of this study was started in 2004. Donors and controls in the pilot study were given the opportunity to continue on in the main study once it started in 2009.

NCT ID: NCT00935987 Completed - Clinical trials for Primary Myelofibrosis

Safety and Efficacy Study of CYT387 in Primary Myelofibrosis (PMF) or Post-polycythemia Vera (PV) or Post-essential Thrombocythemia (ET)

Start date: November 2009
Phase: Phase 1/Phase 2
Study type: Interventional

This study seeks to (i) determine a safe and tolerated dose of CYT387 (momelotinib) given to patients with PMF, post-PV or post-ET and, (ii) assess the effectiveness of orally-administered CYT387 as a treatment for PMF, post-PV or post-ET.

NCT ID: NCT00935168 Completed - Intensive Care Clinical Trials

Crystalloid Versus Hydroxyethyl Starch Trials

CHEST
Start date: December 2009
Phase: Phase 3
Study type: Interventional

The aim of this study is to determine whether patients in the Intensive Care Unit who receive fluid resuscitation with either hydroxyethyl starch (a synthetic colloid solution) or saline (a salt solution), have an increased rate of survival at 90 days.

NCT ID: NCT00934388 Not yet recruiting - Chronic Groin Pain Clinical Trials

A Randomised, Blinded Study on Laparoscopic Mesh Reinforcement for Chronic Groin Pain

Start date: January 2011
Phase: Phase 3
Study type: Interventional

Chronic groin pain is a frequent cause for referral to general surgeons. In some cases this pain may be due to the presence of a hernia. However, if on clinical examination there is no palpable lump or bulge, the cause of the pain may be difficult to elucidate. Some of these patients may have the diagnosis of sportsman's groin. Other names which have been attached to this condition include Gilmores groin and sportsmans hernia. These conditions are more commonly associated with sportsmen and women but those who do not play sport may also receive this diagnosis. Sportsman's groin is thought to be a syndrome of weakness of the posterior inguinal wall without a clinically recognisable hernia. Differing explanations for sportsman's groin include avulsion of the conjoint tendon from the pubic tubercle, weakening of the transversalis fascia, tears in the internal or external oblique, superficial inguinal ring dilatation and abnormalities of the rectus abdominus insertion. There is some evidence that pre peritoneal mesh placement in these patients may be beneficial. The theory being that the mesh prevents pressure transmission to the damages structures, allowing them to heal more rapidly. Aim. To assess the potential benefit of pre peritoneal mesh placement using the TAPP technique in patients with chronic groin pain.

NCT ID: NCT00933348 Suspended - Pressure Ulcer Clinical Trials

Safety and Efficacy of the Fruit-based Product OPAL A for the Treatment of Chronic Venous and Pressure Ulcers

Start date: January 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to examine the safety and efficacy of the fruit-based product OPAL A for the treatment of chronic venous and pressure ulcers.