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NCT ID: NCT00220974 Completed - Clinical trials for Hypercholesterolemia

Study to Assess if Internet-Based Tailored Advice Could Modify Behaviour to Improve Health

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

The purpose of this trial is to find out if a special website might help people discover if they have high cholesterol and then enable them to manage their cholesterol more appropriately. The primary aim of this trial is to determine the effects on consumers' use of cholesterol lowering therapy of an online service that provides automated, individually tailored, advice about eligibility for cholesterol lowering treatment. The primary null hypothesis being tested is that the service will result in no change in the use of cholesterol lowering treatments by consumers that use the service. The secondary aim of the trial is to see if it is possible to improve the cholesterol management of the friends or relatives of consumers that use the I-CAT service. The corresponding secondary null hypothesis being tested is that the I-CAT service will result in no change in the use of cholesterol lowering treatments by the friends or relatives of the consumers that use the service.

NCT ID: NCT00219843 Completed - Melanoma Clinical Trials

Intralesional PV-10 Chemoablation of Metastatic Melanoma

Start date: August 2005
Phase: Phase 1
Study type: Interventional

The objective of this study is to investigate the safety of intralesional (IL) PV-10 for the treatment of metastatic melanoma. This study will also include a preliminary assessment of response of treated and untreated lesions by clinical evaluation at follow-up of 12 to 24 weeks following IL PV-10 treatment.

NCT ID: NCT00219635 Completed - Ejaculation Clinical Trials

Assessment Of Efficacy and Safety UK-390,957 In Men With Premature Ejaculation

Start date: January 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Assessment of efficacy and safety UK-390,957

NCT ID: NCT00219609 Completed - Ejaculation Clinical Trials

Assessment Of Safety Of UK-390,957

Start date: January 2005
Phase: Phase 2/Phase 3
Study type: Interventional

To determine whether UK-390,957 is a safe treatment for premature ejaculation.

NCT ID: NCT00219583 Completed - Ejaculation Clinical Trials

Assessment Of Efficacy and Safety Of UK-390,957 In Men With Premature Ejaculation

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

Assessment of efficacy and safety UK-390,957.

NCT ID: NCT00216736 Completed - Migraine Clinical Trials

Oral Dexamethasone for Treatment of Migraine

Start date: April 2005
Phase: Phase 4
Study type: Interventional

The aim of this project is to determine if a single dose of oral dexamethasone at the time of discharge from the emergency department (ED) [after successful treatment] prevents rebound headache. Hypothesis: That single dose oral dexamethasone 8mg reduces the proportion of patients who suffer rebound headache after treatment for migraine in the ED.

NCT ID: NCT00216411 Completed - Clinical trials for Cerebrovascular Accident

Effects on Quality of Life Following Dysport Treatment in Post-stroke Spasticity of the Arm

Start date: November 2004
Phase: Phase 4
Study type: Interventional

The main purpose of this study is to assess the effect on Quality of Life of two cycles of Dysport treatment on post-stroke spasticity of the upper limb. The effect of treatment on spasticity and function will also be measured.

NCT ID: NCT00216398 Completed - Acromegaly Clinical Trials

Lanreotide Autogel in Patients With Acromegaly Previously Treated With Octreotide LAR

Start date: June 2004
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the efficacy, safety and patient acceptability of Somatuline Autogel in patients with acromegaly previously treated with octreotide LAR.

NCT ID: NCT00216190 Completed - Clinical trials for Mechanically Ventilated and Intubated Subjects

A Safety and Efficacy Study of Dexmedetomidine in ICU Patients Requiring Continuous Sedation

Start date: March 2005
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of dexmedetomidine in ICU subjects who are initially intubated, mechanically ventilated and require sedation for beyond 24 hours.

NCT ID: NCT00214773 Completed - Clinical trials for Mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy Syndrome)

Mucopolysaccharidosis (MPS) VI Clinical Surveillance Program (CSP)

Start date: July 2005
Phase:
Study type: Observational

The objectives of this program are: to further characterize the natural progression of MPS VI disease; to generate and disseminate information on the care and management of MPS VI patients to clinical and medical professionals; to provide a resource to physicians and patients by providing information for optimizing patient care based on aggregate data; to characterize the clinical response to long-term Naglazyme® (galsulfase) treatment; to further characterize the long-term safety of Naglazyme® treatment.