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NCT ID: NCT00628576 Completed - Clinical trials for Deep Venous Thrombosis

Evaluation of Long-Term Sequelae After Thrombophlebitis, i.e. Deep Venous Thrombosis of the Lower Extremities

Start date: October 1993
Phase: Phase 3
Study type: Interventional

The purpose of the study was to evaluate efficacy and safety of the new acute treatment of deep venous thrombosis by use of low-molecular-weight heparin compared with standard treatment using unfractionated heparin, especially concerning long-term morbidity.

NCT ID: NCT00628004 Completed - Leg Ulcers Clinical Trials

Safety Evaluation of Biatain Ibu in Painful Chronic Venous Leg Ulcers

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

The objective of this open label extension study (extension to study DK143WS) is to evaluate the safety of Biatain Ibu during 6 -12 weeks of exposure and during a 40 - 46 weeks safety follow-up period.

NCT ID: NCT00627406 Completed - Clinical trials for OHSS (Ovarian Hyperstimulation)

Triggering of Final Oocyte Maturation With GnRHa (Buserelin) in GnRH Antagonist Cycles

Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to possibly further improve the clinical outcome and explore the incidence of OHSS in patients, who have final oocyte maturation with GnRHa (Buserelin) in GnRH antagonist IVF/ICSI cycles

NCT ID: NCT00627289 Completed - Pain Clinical Trials

Selective Neurectomy and Mesh Removal for Chronic Postherniotomy Pain

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

Chronic postherniotomy pain affects every day activities in 5-8% of patients. However, no established treatment for this pain syndrome exists and previous reports on the effect of surgical intervention suffer from methodological problems. The neurophysiological characteristics suggest that pain arises from deeper neuronal structures injured during surgery or by ongoing inflammation from the mesh. This study investigates the effect of removing inserted mesh and compressed nerves on pain related daily impairment of activities assessed by the validated AAS questionnaire before and 6 months after surgery

NCT ID: NCT00626353 Completed - Acute Stroke Clinical Trials

Interdisciplinary Home Rehabilitation of Patients With Stroke. A Randomised Controlled Intervention Trial.

Start date: July 2007
Phase: N/A
Study type: Interventional

Objective: To evaluate the effect of interdisciplinary home rehabilitation of patients with acute stroke. The trial seeks to evaluate: 1. Can early home rehabilitation affect the degree of independence (motor capacity, activities of daily living and cognitive status), quality of life and the possibility of discharge to own home? 2. Can home rehabilitation influence the length of admission at a rehabilitation centre in the municipality, readmission to hospital, the use of healthcare services and death? 3. To what extend can home rehabilitation be implemented according to finances? Materials and methods: Patients at the age 18 years or more admitted to the stroke unit at the University Hospital of Gentofte. The patients were eligible when meeting the following criteria: symptoms of stroke, need of rehabilitation tree days after admission, living in own home in the Municipality of Gentofte, Lyngby-Taarbaek or Rudersdal and Modified Rankin Score between 0 and 3. The trial was conducted as a randomised controlled trial. The control group patients were rehabilitated according to normal procedure. The intervention group patients were rehabilitated according to normal procedure and were additionally rehabilitated at home during admission and four weeks after discharge.

NCT ID: NCT00626002 Completed - Clinical trials for Moderate to Severe Plaque Psoriasis

Open Label Continuation Study in Moderate to Severe Psoriasis

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate long term safety, efficacy and tolerability of ABT-874 in adults with moderate to severe psoriasis.

NCT ID: NCT00625157 Completed - Clinical trials for Discoid Lupus Erythematosus

Efficacy and Safety of ASF-1096 Cream 0.5% in the Treatment of Discoid Lupus Erythematosus (DLE) Lesions (2)

Start date: n/a
Phase: Phase 2
Study type: Interventional

Lupus Erythematosus (LE) is an autoimmune disorder that includes a broad spectrum of clinical forms. One of these forms, Discoid Lupus Erythematosus (DLE) is a chronic disfiguring disease confined to the skin. The aim of this pivotal trial is to investigate the efficacy and safety of ASF-1096 cream 0.5% in the treatment of patients with DLE or SLE presenting newly developed discoid lesions.

NCT ID: NCT00624169 Completed - Clinical trials for Peptic Ulcer Perforation

Peptic Ulcer Perforation Study

PULP
Start date: November 2007
Phase: N/A
Study type: Interventional

The objective of this study is to implement an optimized perioperative course for patients surgically treated for peptic ulcer perforation in order to improve the outcome for these patients. The optimized perioperative course consists of a number of interventions carried out before, during and after surgery.

NCT ID: NCT00624104 Completed - Obesity Clinical Trials

VLDL-triglyceride Under Acute Hyperinsulinaemia

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

The purpose of the study is to investigate and compare the lipid metabolism in lean and obese individuals. We want to investigate the effect of postprandial hyperinsulinaemia on VLDL-triglyceride metabolism

NCT ID: NCT00623779 Completed - Clinical trials for Persistent or Permanent Non-valvular Atrial Fibrillation

Atrial Fibrillation (AF) Patients Not Taking Vitamin-K Antagonist (VKA)

Start date: October 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the safety and tolerability of AZD0837 in patients with atrial fibrillation who are unable or unwilling to take vitamin K antagonist therapy for up to 3 months.