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24 studies found for:    Porencephaly

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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 Recruiting COL4A1 Gene Related Cerebra-retinal Angiopathy
Condition: Cerebra-retinal Angiopathy
Intervention: Genetic: COL4A1 genetic testing
3 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)
4 Recruiting Transcranial Direct Current Stimulation in a Smoking Cessation Trial
Condition: Nicotine Dependence
Intervention: Device: SmartStim Model 200 tDCS Device
5 Active, not recruiting
Has Results 		Levonorgestrel Contraceptive Intrauterine Systems (LCS) Pearl Index Study
Condition: Contraception
Interventions: Drug: LCS12;   Drug: LCS16
6 Unknown † A Clinical Trial of a Self-Management Education Program for People With Chronic Stable Angina
Condition: Chronic Stable Angina
Intervention: Behavioral: Psychoeducation
7 Not yet recruiting Effect of Omega-3 Phospholipids on Perceptual-cognitive Training
Condition: Cognition - Other
Intervention: Dietary Supplement: Omega-3
8 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)
9 Completed Study Evaluating Combination of Levonorgestrel (LNG) and Ethinyl Estradiol (EE) in Premenstrual Dysphoric Disorder
Conditions: Menstruation Disturbances;   Premenstrual Syndrome
Intervention: Drug: levonorgestrel/ethinyl estradiol
10 Completed
Has Results 		Cardiac Home Education and Support Trial (CHEST): A Pilot Study
Condition: Coronary Artery Disease
Intervention: Other: Peer Support
11 Completed Topical DHEA Against Vaginal Atrophy
Condition: Vaginal Atrophy
Interventions: Drug: Placebo;   Drug: DHEA (0.25%);   Drug: DHEA (0.5%);   Drug: DHEA (1.0%)
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 Not yet recruiting The Influence of Energy Drinks on the Blood Oxygenation Concentration of the Optic Nerve
Condition: Healthy
Intervention: Drug: Redbull, energy drink
14 Completed
Has Results 		Efficacy and Safety Study for the Treatment of Dysfunctional Uterine Bleeding
Condition: Metrorrhagia
Interventions: Drug: Estradiol valerate/Dienogest (Natazia, Qlaira, BAY86-5027);   Drug: Placebo
15 Completed
Has Results 		Distribution of Bupropion and Varenicline to Increase Smoking Cessation Attempts
Conditions: Tobacco Use Disorder;   Smoking;   Smoking Cessation
Interventions: Drug: bupropion;   Drug: varenicline;   Behavioral: motivational emails
16 Completed Study Evaluating PD-0299685 for the Treatment of Vasomotor Symptoms (Hot Flashes / Flushes) Associated With Menopause
Condition: Hot Flashes
Intervention: Drug: PD-0299685
17 Not yet recruiting Partnership for Applied Research in Fracture Prevention Programs for the Elderly
Condition: Osteoporosis With Current Fragility Fracture
Intervention: Other: Integrated program
18 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)
19 Not yet recruiting Effect of Travoprost 0.004% on Retinal Oximetry in Primary Open Angle Glaucoma
Condition: Primary Open Angle Glaucoma
Interventions: Drug: placebo;   Drug: travoprost
20 Completed Efficacy and Safety Study of an Oral Contraceptive in Healthy Females
Condition: Contraception
Intervention: Drug: EV/DNG (Qlaira, BAY86-5027, SH T00658ID)
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† Indicates status has not been verified in more than two years