317 studies found for:    GENITOURINARY TRACT ANOMALIES
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Rank Status Study
1 Completed Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions
Conditions: WAGR Syndrome;   Wilm's Tumor;   Aniridia;   Urogenital Abnormalities;   Mental Retardation
Intervention:
2 Withdrawn CDB-2914 for Abnormal Uterine Bleeding in Premenopausal Women
Condition: Urogenital Abnormalities
Intervention: Drug: CDB-2914
3 Withdrawn Safety, Pharmacokinetics and Pharmacodynamics of NBI-77860 in Adolescent Females With Congenital Adrenal Hyperplasia
Condition: Congenital Adrenal Hyperplasia
Intervention: Drug: NBI-77860
4 Unknown  Biomechanical Assessment of Level Gait in Patient's Status Post Bladder Exstrophy
Condition: Bladder Exstrophy
Intervention:
5 Recruiting Prevalence of Congenital Uterine Malformations
Condition: Congenital Uterine Anomalies
Intervention:
6 Terminated The Impact of Treating Minor Uterine Cavity Abnormalities Diagnosed by Office Hysteroscopy in Unselected In Vitro Fertilization (IVF) Cases
Condition: Minor Intra-uterine Abnormalities
Interventions: Procedure: Treatment of predefined abnormality by hysteroscopic surgery;   Drug: Ofloxacinum/Doxycycline
7 Unknown  Long Term Outcome of Congenital Solitary Kidney
Condition: Congenital Solitary Kidney
Intervention:
8 Recruiting Diagnostic Relevance of Laser Confocal Microscopy for the Screening of Upper Urinary Tract Tumors
Conditions: Hematuria,;   Nephrolithiasis;   Cancer of Urinary Tract;   Ureteropelvic Junction Obstruction
Intervention: Device: Laser confocal microscopy
9 Recruiting AVAST Anomalies Vasculaires Associées au Syndrome de Turner (Vascular Abnormalities Associated With Turner Syndrome)
Conditions: Turner Syndrome;   Peripheral Angiopathy;   Vascular Malformation;   Lymphedema
Intervention: Procedure: Echo doppler
10 Unknown  Non-Invasive Determination of Fetal Chromosome Abnormalities
Conditions: Down Syndrome (Trisomy 21);   Edward's Syndrome (Trisomy 18);   Patau Syndrome (Trisomy 13);   Klinefelter Syndrome (47, XXY);   and Other Chromosome;   Abnormalities.
Intervention:
11 Completed The Effects of Estrogen on Cognition in Girls With Turner Syndrome
Conditions: Gonadal Dysgenesis;   Turner's Syndrome
Intervention: Behavioral: cognitive tests and scales
12 Completed Effect of Biosynthetic Growth Hormone and/or Ethinyl Estradiol on Adult Height in Patients With Turner Syndrome
Conditions: Gonadal Dysgenesis;   Turner's Syndrome
Intervention: Drug: Growth Hormone (Humatrope)
13 Completed The Caudal Space in Children: Ultrasound Evaluation
Conditions: Hydrocele;   Inguinal Hernia;   Hypospadia;   Cryptorchidism;   Genitourinary Disease
Intervention: Other: ultrasound evaluation of caudal space
14 Recruiting Study of Smith-Lemli-Opitz Syndrome
Conditions: Abnormalities;   Inborn Errors of Metabolism;   Mental Retardation;   Muscle Hypotonia;   Smith Lemli Opitz Syndrome
Intervention:
15 Recruiting SNP-based Microdeletion and Aneuploidy RegisTry (SMART)
Conditions: 22q11 Deletion Syndrome;   DiGeorge Syndrome;   Trisomy 21;   Trisomy 18;   Trisomy 13;   Monosomy X;   Sex Chromosome Abnormalities;   Cri-du-Chat Syndrome;   Angelman Syndrome;   Prader-Willi Syndrome;   1p36 Deletion Syndrome
Intervention:
16 Completed Dry Eye in Women With Turner Syndrome and Women With Premature Ovarian Failure
Conditions: Turner Syndrome;   Ovarian Failure, Premature;   Sex Chromosome Aberrations;   Menopause;   Perimenopause
Intervention:
17 Active, not recruiting National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions
Conditions: Marfan Syndrome;   Turner Syndrome;   Ehlers-Danlos Syndrome;   Loeys-Dietz Syndrome;   FBN1, TGFBR1, TGFBR2, ACTA2 or MYH11 Genetic Mutation;   Bicuspid Aortic Valve Without Known Family History;   Bicuspid Aortic Valve With Family History;   Bicuspid Aortic Valve With Coarctation;   Familial Thoracic Aortic Aneurysm and Dissections;   Shprintzen-Goldberg Syndrome;   Other Aneur/Diss of Thoracic Aorta Not Due to Trauma, <50yo;   Other Congenital Heart Disease
Intervention:
18 Recruiting Expanded Noninvasive Genomic Medical Assessment: The Enigma Study
Conditions: Down Syndrome;   Edwards Syndrome;   Patau Syndrome;   Klinefelter Syndrome;   Turner Syndrome;   DiGeorge Syndrome;   Chromosome Deletion;   Aneuploidy
Intervention: Other: Blood sampling for Laboratory Developed Test (LDT) analysis
19 Recruiting Whole Blood Specimen Collection From Pregnant Subjects
Conditions: Down Syndrome;   Edwards Syndrome;   Patau Syndrome;   Klinefelter Syndrome;   Turner Syndrome;   DiGeorge Syndrome;   Perinatal Infections
Intervention: Other: Observational - no intervention
20 Recruiting Micro RNAs as a Marker of Aortic Aneurysm in Hereditary Aortopathy Syndromes
Conditions: Marfan Syndrome;   Loeys-Dietz Syndrome;   Thoracic Aortic Aneurysm and Dissection Syndromes;   Ehlers-Danlos Type IV Syndrome;   Turner Syndrome
Intervention:

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Indicates status has not been verified in more than two years