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NCT ID: NCT00228280 Active, not recruiting - Alveolar Bone Loss Clinical Trials

Periapical Bone Healing After Apicectomy With and Without Retrograde Root Filling

Start date: January 2005
Phase: Phase 1/Phase 2
Study type: Interventional

Ph.D project: Periapical bone healing after apicectomy with and without retrograde root filling. The aim of this study is to assess periapical bone healing after apicectomy without a filling and apicectomy combined with a retrograde filling material, MTA. Further, we will estimate risk factors in non-healing cases. Study hypothesis: There is no difference in treatment outcome between: Periapical bone healing after apicectomy with retrograde root filling and Periapical bone healing after apicectomy without retrograde root filling

NCT ID: NCT00228241 Active, not recruiting - Sick Sinus Syndrome Clinical Trials

Left Ventricular Function and Remodelling During Permanent Pacing

Start date: September 2003
Phase: N/A
Study type: Interventional

1. Background - Pacemaker treatment gives asynchronous activation of the heart that often results in decreased heart function and clinical heart failure. New pacemaker types that stimulates both left and right ventricle ( biventricular pacemakers ) is introduced to the treatment of patients with heart failure, decreased left ventricular function and ECG signs with left bundle branch block. 2. Hypothesis - Ventricular pacing results in remodelling of the left ventricle and decreased left ventricular function. Biventricular pacing do not do this. Ventricular pacing results in heart failure and increased wall stress with decreased 6 minutes walk test and increased BNP in blood samples. This is not seen by biventricular pacing. 3. Materials and methods - 3 studies. All patients are examined by echocardiography 2-dimensional, M-mode, 3-dimensional and with tissue harmonic imaging. Study 1) Patients with AV-conduction disorder that needs pacemaker treatment are randomized to DDD-pacemaker or biventricular pacemaker. Study 2) Patients with sick sinus syndrome included in DANPACE are randomized to AAI- or DDD-pacemaker. Study 3 ) Acute study to examine the changes in patients AV-block before DDD-pacemaker implantation and after implantation.

NCT ID: NCT00226603 Active, not recruiting - Clinical trials for Groin Injuries in Football Players

Lyske Trial (Danish) Groin Trial

Start date: September 1997
Phase: Phase 2/Phase 3
Study type: Interventional

To examine the effect of a specific training programme towards groin injuries in male footbal players. To evaluate the effect on other football related injuries as well. To examine any possible relations between various possible predictors such as experience, age, hypermobility and others, and the risk of sustaining inujries during football.

NCT ID: NCT00225641 Active, not recruiting - Colorectal Cancer Clinical Trials

Assessment of Frequency of Surveillance After Curative Resection in Patients With Stage II and III Colorectal Cancer

Start date: March 2006
Phase: N/A
Study type: Interventional

The aim is to conduct a prospective multicentre randomised study comparing two different control regimens after resection for colorectal cancer stage II - III. Follow-up after surgery for colorectal cancer is a controversial issue. The reasons for follow-up are: to obtain a better overall survival, for scientific purposes and/or for psychological reasons and/or as quality assessment. Meta-analyses of randomised controlled studies have lately shown that a beneficial effect on the overall mortality could be found with intense follow-up compared to sporadic. This study compares the regimen of CT-scan or MR scan of the liver, control of the carcinoembryonic antigen (CEA), and CT-scan or X-ray of the lungs in two groups with either control after 12 and 36 months, or after 6, 12, 18, 24, and 36 months. The efficacy parameters are total and cancer-specific mortality.

NCT ID: NCT00225602 Active, not recruiting - Schizophrenia Clinical Trials

Assertive Community Treatment in Copenhagen

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

The aim of the study is to evaluate the effect of assertive community treatment in Copenhagen in two regions compared with two regions where this treatment was not implemented. The effect on user satisfaction, use of bed days, social network, global assessment of functioning, substance misuse will be evaluated.

NCT ID: NCT00221585 Active, not recruiting - Schizophrenia Clinical Trials

The National Danish Schizophrenia Project

Start date: October 1997
Phase: N/A
Study type: Observational

A prospective, longitudinal, multi-centre investigation (16 centres), including 562 patients, consecutively referred during two years, with a first-episode psychosis of ICD-10, F-2 type. Patients were treated with: 1) ‘Supportive psychodynamic psychotherapy as a supplement to treatment as usual’, 2) an ‘Integrated, assertive, psychosocial and educational treatment programme’, and 3) ‘Treatment as usual’.

NCT ID: NCT00209209 Active, not recruiting - Clinical trials for Lymphoma, Mantle-Cell

Induction Chemotherapy (R-CHOP Vs. R-FC) Followed by Interferon Maintenance Versus Rituximab Maintenance in MCL

MCLelderly
Start date: January 14, 2004
Phase: Phase 3
Study type: Interventional

The aim of this study is to answer the following independent questions in the treatment of mantle cell lymphomas: - Can rituximab-fludarabine, cyclophosphamide (R-FC) improve the reduction of lymphoma mass compared to rituximab-cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) and so become a new standard for initial cytoreductive therapy? - Can maintenance with rituximab substitute the interferon maintenance and even improve the progression free survival in patients after successful initial cytoreductive therapy?

NCT ID: NCT00197899 Active, not recruiting - Sepsis Clinical Trials

Low-Dose Endotoxemia and the Acute Phase Response

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

The purpuse of this study is to examine the acute phase respons when different doses of E. Coli Endotoxin is injected in healty volunters.

NCT ID: NCT00197847 Active, not recruiting - Sepsis Clinical Trials

Infection Surveillance in Intensive Care Patients

Start date: December 2002
Phase: N/A
Study type: Observational

Purpose of the study is to investigate and quantify known and possible new riskfactors for nosocomiel infection and death in the intensive care setting. As new riskfactors Mannose Binding Lechtin and Procalcitonin are chosen and compared to established riskfactors.

NCT ID: NCT00192985 Active, not recruiting - Trauma Clinical Trials

Does a Nitrofurazone Coated Bladder Catheter Reduce the Number of Urinary Tract Infections in Trauma

Start date: May 2003
Phase: Phase 3
Study type: Interventional

Urinary tract infections occurs in trauma. We investigate whether a nitrofurazone coated can reduce the number of urinary tract infections.