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NCT ID: NCT00495248 Active, not recruiting - Stroke Clinical Trials

Thriving, Activity and Social Participation After Stroke

Start date: January 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to evaluate the effect of a group intervention programme for community dwelling elders with stroke or TIA.The intervention is inspired by a Lifestyle Redesign method developed in the USA. The study is conducted as a multi centre randomized controlled trial. Participants are recruited from five hospitals and the intervention is implemented at six to seven senior centres. The control group is offered physical activity at the senior centre once a week. The intervention group is offered the same with addition of the programme inspired by Lifestyle Redesign. The study will contribute to knowledge whether the intervention will promote social participation and thriving in daily life and prevent social isolation and depressive symptoms among community dwelling elders with stroke or TIA.

NCT ID: NCT00491673 Active, not recruiting - Clinical trials for Femoral Neck Fractures

A Prospective Randomized Trial of Uncemented Versus Cemented Hemiarthroplasty for Displaced Femoral Neck Fractures

HEMI04
Start date: September 2004
Phase: N/A
Study type: Interventional

There is increasing evidence that primary hemiarthroplasty is the treatment of choice for displaced femoral neck fractures in the elderly No definite conclusions have been made in regards to what kind of arthroplasty is favourable Cemented implants are associated with increased risk of perioperative cardiovascular incidents and increased mortality. Cementless implants are associated with increased postoperative pain and decreased walking ability. This study investigates the differences between one well-documented cemented femoral stem and one well-documented uncemented femoral stem. Previous studies have mostly used uncemented stems with different designs. Null hypothesis: No (less than 10 points) difference in HHS between groups at 1 year and 5 years

NCT ID: NCT00490594 Active, not recruiting - Knee Injuries Clinical Trials

SeriACLâ„¢ Device Trial for Anterior Cruciate Ligament (ACL) Reconstruction

Start date: June 2007
Phase: Phase 1
Study type: Interventional

The SeriACL device was developed as an alternative to an autograft (i.e., tissue that is taken from a patient's own body) or an allograft (i.e., tissue that is taken from a cadaver) for ACL reconstruction. The SeriACL device is made of silk yarns, knit and processed with SeriCoatâ„¢ surface treatment which makes it easier to wet the material. The SeriACL device is designed to be a temporary support structure to replace the torn ACL and to stabilize the knee joint following surgical repair. It is designed to use the body's own healing process to regenerate the patient's own new ligament tissue. As the new tissue grows and the support structure is needed less over time, the SeriACL device is bioresorbed (i.e., broken down) by the patient's body. The SeriACL device is designed to be installed with standard surgical techniques for ACL repair. This study is designed to test the safety of the SeriACL device in primary total ACL repair in patients with a torn ACL. The study will evaluate whether repair of the ACL with the SeriACL device will return the knee to normal function and what, if any, side effects will occur.

NCT ID: NCT00423982 Active, not recruiting - Clinical trials for Staphylococcal Infections

Rifampin Combination Therapy Versus Monotherapy in Early Staphylococcal Infections After Total Hip and Knee Arthroplasty

Start date: April 2006
Phase: Phase 4
Study type: Interventional

The number of patients requiring joint replacement is increasing due to its success in restoring function and pain relief, and the growing population of the elderly. One of the most serious complications of arthroplasty is joint prosthesis infection. Due to the absence of prospective, randomized, controlled studies, there is no consensus concerning diagnosis and treatment of prosthetic joint infections. The main objective of this trial is to evaluate the clinical efficacy of rifampin combination therapy versus monotherapy using cloxacillin or vancomycin in early staphylococcal infections after total hip and knee arthroplasty.

NCT ID: NCT00423384 Active, not recruiting - Renal Transplant Clinical Trials

Ibandronate Versus Placebo in the Prevention of Bone Loss After Renal Transplantation.

Start date: January 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Loss of bone mass is a common complication in patients with end-stage-renal failure, both before and particularly after transplantation. In addition to standard underlying therapy with calcium and active vitamin D, we will study the effect of ibandronate (a bisphosphonate) versus placebo on bone mineral density as well as incidence of fracture rates after kidney transplantation.We also wish to study whether any prevented bone loss will also lead to reduced cardiovascular disease. Patients will be followed for 12 months after transplantation, and the ibandronate treatment is one injection every 3 months.

NCT ID: NCT00393614 Active, not recruiting - CSWS Clinical Trials

Levetiracetam Treatment of Children With Subclinical Sleep-Activated Epileptiform Activity (SSEA)

Start date: May 2007
Phase: Phase 4
Study type: Interventional

In clinical practice at the National centre for epilepsy (SSE) in Norway we see many children who have subclinical epileptiform activity in EEG that increases substantially during slow wave sleep (SSEA; subclinical sleep-activated epileptiform activity). They may or may not have seizures. Hence, according to the definition some children with SSEA do not suffer from epilepsy because they do not experience seizures. Many of these children have symptoms such as: attention deficit hyperactivity disorders (AD/HD), dyslectic problems, sleep problems, tantrums or autistic symptoms . We hypothesize that this subclinical epileptiform activity during slow sleep may act negatively on cognitive functions, language and behaviour in some children; even when the spike-wave discharges are less frequent than in CSWS (continuous spike-waves during slow sleep).

NCT ID: NCT00378248 Active, not recruiting - Clinical trials for Personality Disorders

Ullevål PersonalityProject

Start date: May 2004
Phase: N/A
Study type: Interventional

Ullevål PersonalityProject is a ranomized controlled trial of treatment of patients with personality disorder. It's main purpose is to test the effect of a long-term combined treatment program compared with eclectic individual therapy for patients with personality disorders. The main study hypothesis is that long-term combined treatment is superior to eclectic individual therapy with respect to improvement in personality functioning, psychosocial functioning, symptoms, interpersonal problems, and self destructive behavior for poorly functioning patients with personality disorders.

NCT ID: NCT00327912 Active, not recruiting - Obesity Clinical Trials

Laparoscopic Roux-en-Y Gastric Bypass Versus Laparoscopic Biliopancreatic Diversion (BPD)- Duodenal Switch for Superobesity

ASGARD
Start date: April 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the outcome in a broad perspective after laparoscopic Roux-en-Y gastric bypass and laparoscopic BPD-duodenal switch in the treatment of superobesity (body mass index [BMI] > 50 kg/m2).

NCT ID: NCT00303537 Active, not recruiting - Fatty Liver Clinical Trials

Metformin in Non-Alcoholic Fatty Liver Disease

Start date: November 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The study evaluates the use of the antidiabetic medicine metformin in nonalcoholic fatty liver disease.

NCT ID: NCT00294827 Active, not recruiting - Colo-rectal Cancer Clinical Trials

Liver Transplantation and Metastatic Colo-rectal Cancer.

Start date: February 2006
Phase: Phase 2
Study type: Interventional

Survival of colo-rectal cancer patients after liver transplantation.