Comment Period Extended to 3/23/2015 for Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials
29 studies found for:    Porencephaly
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Study Details
Participant Details
Identifiers
Dates
Rank Status Study
1 Completed Study of Abnormal Blood Clotting in Children With Stroke
Conditions: Abnormalities;   Blood Coagulation Disorder;   Brain Disease;   Cerebrovascular Accident;   Vascular Disease
Intervention:
2 Active, not recruiting COL4A1 Gene Related Cerebra-retinal Angiopathy
Condition: Cerebra-retinal Angiopathy
Intervention: Genetic: COL4A1 genetic testing
3 Recruiting To Look at the Characteristics of Synovial Fluid and Cartilage Matrix in Osteoarthritic Knee After Hyaluronic Acid Injection
Condition: Knee Osteoarthritis
Interventions: Drug: Euflexxa;   Device: Magnetic Resonance Imaging (MRI)
4 Completed IDEAL Study: Identification of the Determinants of the Efficacy of Arterial Blood Pressure Lowering Drugs
Condition: Hypertension
Interventions: Drug: Indapamide (T2);   Drug: Perindopril (T1);   Drug: Placebo of Perindopril (P1);   Drug: Placebo of Indapamide (P2)
5 Recruiting Effect of Omega-3 Phospholipids on Perceptual-cognitive Training
Condition: Cognition - Other
Interventions: Dietary Supplement: Omega-3;   Other: Placebo
6 Unknown  Effect of Travoprost 0.004% on Retinal Oximetry in Primary Open Angle Glaucoma
Condition: Primary Open Angle Glaucoma
Interventions: Drug: placebo;   Drug: travoprost
7 Recruiting Clinical Investigation on the Blood Oxygenation at the Optic Nerve Head in Fabry Patients
Condition: Fabry Disease
Interventions: Procedure: Contrast sensitivity measurement;   Procedure: Slit Lamp assessment and intra-ocular pressure measurement;   Procedure: Visual field testing;   Procedure: Oxygen flow at the optic nerve head measurement;   Drug: Tropicamide;   Device: OSOME
8 Recruiting Canadian Humira Post Marketing Observational Epidemiological Study: Assessing Effectiveness in Ankylosing Spondylitis
Condition: Ankylosing Spondylitis
Intervention:
9 Completed Topical DHEA Against Vaginal Atrophy
Condition: Vaginal Atrophy
Interventions: Drug: Placebo;   Drug: DHEA (0.25%);   Drug: DHEA (0.5%);   Drug: DHEA (1.0%)
10 Unknown  Donepezil Effect on Visual Attention and Training
Condition: Healthy
Interventions: Drug: Donepezil administration;   Drug: Placebo administration
11 Recruiting The MATCH (Medication Aids for Tobacco Cessation and Health) Study
Conditions: Tobacco Use Disorder;   Nicotine Dependence
Interventions: Drug: Bupropion;   Drug: Varenicline;   Behavioral: Weekly Motivational Emails
12 Completed Testosterone Therapy in Naturally Menopausal Women With Low Sexual Desire Receiving Transdermal Estrogen
Condition: Hypoactive Sexual Desire Disorder
Interventions: Drug: Testosterone;   Drug: Placebo
13 Completed Efficacy and Safety Study of an Oral Contraceptive in Healthy Females
Condition: Contraception
Intervention: Drug: EV/DNG (Qlaira, BAY86-5027, SH T00658ID)
14 Completed
Has Results
Cardiac Home Education and Support Trial (CHEST): A Pilot Study
Condition: Coronary Artery Disease
Intervention: Other: Peer Support
15 Recruiting Partnership for Applied Research in Fracture Prevention Programs for the Elderly
Condition: Osteoporosis With Current Fragility Fracture
Intervention: Other: Integrated program
16 Completed Study Evaluating Conjugated Estrogen Cream for Atrophic Vaginitis
Conditions: Atrophic Vaginitis;   Atrophy;   Vaginitis
Interventions: Drug: PVC (daily for 21 days, 7 days off);   Drug: PVC (twice weekly)
17 Suspended Transcranial Direct Current Stimulation in a Smoking Cessation Trial
Condition: Nicotine Dependence
Interventions: Device: active transcranial Direct Current Stimulation;   Device: sham transcranial Direct Current Stimulation
18 Unknown  A Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina
Condition: Chronic Stable Angina
Intervention: Behavioral: Psychoeducation
19 Completed
Has Results
Study in Women With Idiopathic Menorrhagia to Determine the Reduction in Menstrual Blood Loss (MBL) After Treatment With the Levonorgestrel-releasing Intrauterine System (IUS)
Condition: Menorrhagia
Interventions: Drug: Levonorgestrel IUS (Mirena, BAY86-5028);   Drug: Medroxyprogesterone acetate
20 Completed
Has Results
Study on Safety and Efficacy of an Oral Contraceptive in Long Cycles
Condition: Contraception
Interventions: Drug: Flexible (extended) treatment of EE20/DRSP (YAZ, BAY86-5300);   Drug: Fixed extended treatment of EE20/DRSP (YAZ, BAY86-5300);   Drug: Standard 24+4 treatment of EE20/DRSP (YAZ, BAY86-5300)

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Indicates status has not been verified in more than two years