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Ethikkommission der Medizinischen Universität Wien

A 36-week, double blind, parallel group, multicenter study to compare the efficacy and safety of piracetam with placebo in children with developmental reading disorder (dyslexia). Clinical first-in-human dose escalation study evaluating the safety and tolerability of intranodal administration of an RNA-based cancer vaccine targeting the tumor-associated antigens NY-ESO-1 and tyrosinase in patients with advanced melanoma. Investigation of cardiac status of adult patients receiving anti-cancer therapy in childhood with 2D speckle tracking echocardiography. Pilot Study. A Randomized Phase III study comparing conventional chemotherapy to low dose total body irradiation-based conditioning and hematopoietic cell transplantation from related and unrelated donors as consolidation therapy for older Patients with AML in first Complete Remission.

Study to determine the safety and efficacy of long-term administration of Alupent syrup for the treatment of bronchial asthma in children. Study to determine the safety and efficacy of long term administration of Alupent syrup for the treatment of bronchial asthma in children. The objective of this study was to document the efficacy and tolerability of the new formulation of Andriol Testocaps in the treatment of late-onset hypogonadism in a clinical practice setting.

Use of piracetam in the treatment of children with the infantile brain-damage syndrome. Use of piracetam in the treatment of children with severe drug poisoning. Statistical report of a controlled clinical study regarding the influence of piracetam upon the symptoms presented by children with learning disabilities. Study to determine the safety and efficacy of long-term administration of Alupent syrup to children. A single dose study to compare the efficacy of acetaminophen sustained release pediatric chewable tablets to ibuprofen suspension in febrile children.

We tested the oral form of testosterone, testosterone undecanoate (Andriol, NV Organon, The Netherlands), in men with PADAM and evaluated its efficacy and safety in Korean male patients. Testosterone replacement with long-acting Testopel pellets had a lower rate of infection (0.3%, 1/292 procedures) as compared with historical data from the Organon testosterone pellet (1.4-6.8%). Additionally, the rate of pellet extrusion was substantially lower (0.3%, 1/292 procedures) as compared with historical data (8.5-12%).

ALFApump system versus large volume paracentesis in the treatment of refractory ascites. A multicentre randomised controlled study. Determination of the pharmacokinetics and safety of risperidone at steady state in children and adolescents 5 to less than 18 years of age.

An Open-Label, Uncontrolled Pharmacokinetic and Clinical Evaluation Study of Valaciclovir Hydrochloride in Children with Chickenpox. Randomised study to investigate the effects on growth, on uraemic toxins profile and on the safety of recombinant human growth hormone treatment in very young children with growth retardation secondary to chronic renal insufficiency (CRI). A phase II study of vinorelbine tartrate in children with Recurrent or Refractory Malignancies. Variant pathogenetic therapy in the acute phase of hypoxic-traumatic brain damage in immature children.

Randomised Study to Investigate the Effects on Growth, on Uremic Toxins Profile and on Renal Function of Recombinant Human Growth Hormone Treatment in Very Young Children With Growth Retardation Secondary To Chronic Renal Insufficiency. Piracetam therapy does not enhance cognitive functioning in children with Down syndrome.

Langzeit-Nachbeobachtungsstudie mit Patienten, die an einer klinischen Studie teilgenommen haben, in der ihnen BMS-914143 zur Behandlung von chronischer Hepatitis C verabreicht wurde A Long-Term Follow-Up Study of Subjects Who Participated in a Clinical Trial in which BMS-914143 was Administered for the Treatment of Chronic Hepatitis C

  • Initiating testosterone treatment had no statistically significant effect on total PSA, free PSA or free/total PSA ratio, and any initial PSA change had no predictive relationship to subsequent diagnosis of cancer.
  • An Open-Label, Uncontrolled Pharmacokinetic and Clinical Evaluation Study of Valaciclovir Hydrochloride in Children with Chickenpox.
  • A single centre study to assess the safety and efficacy of Movicol in the treatment of faecal impaction in children followed by a double-blind randomised phase to compare the safety and efficacy of Movicol and lactulose for maintenance therapy.
  • Dec 1994.
  • Risperidone in the treatment of disruptive behavior disorders in children with intellectual limitations.
  • A Phase III Multiple Dose Use Study of APAP Extended Release Pediatric Suspension Compared to Children’s Tylenol Elixir in the Treatment of Febrile Children.

Dec 1994.A single dose study to compare the efficacy of acetaminophen sustained release pediatric chewable tablets to ibuprofen suspension in febrile children. Dec 1994. A phase III double-blind, single dose study of the comparative antipyretic effectiveness and safety of standard and double standard (C-47) doses of acetaminophen in febrile children. Jan 1984.A phase III double-blind, single dose study of the comparative antipyretic effectiveness and safety of standard and double standard (C-47) doses of acetaminophen in febrile children. Jan 1984.

Symptoms and signs consistent with androgen deficiency and low testosterone levels are recognized frequently in clinical practice. Recent population-based epidemiological studies indicate that low testosterone levels in men are associated with increased morbidity and mortality.

A single centre study to assess the safety and efficacy of Movicol in the treatment of faecal impaction in children followed by a double-blind randomised phase to compare the safety and efficacy of Movicol and lactulose for maintenance therapy. 94-406, Unpublished Report CSR204. May 1997.A Phase III Multiple Dose Use Study of APAP Extended Release Pediatric Suspension Compared to Children’s Tylenol Elixir in the Treatment of Febrile Children. A Phase III Multiple Dose Use Study of APAP Extended Release Pediatric Suspension Compared to Children’s Tylenol Elixir in the Treatment of Febrile Children. A Phase III Multiple Dose Use Study of APAP Extended Release Pediatric Chewable Tablets Compared to Children’s Tylenol Chewable Tablets in the Treatment of Febrile Children.

For men with androgen deficiency on testosterone replacement therapy (TRT), clinical concern relates to the development of prostate cancer (PCa). Early detection of left ventricular dysfunction in patients receiving anticancer therapy for breast cancer with 2D speckle tracking echocardiography and biomarkers. Pilot Study. Exploratory data analysis of retrospective data to evaluate the effect of topical haemostyptica in the treatment of intractable hematuria. Double-blind, randomized clinical study to determine the efficacy of Anaestherit 10% on histamine-induced pruritus and UVB-light induced slight sunburn in healthy subjects.

Toxocara-Infektion des Menschen in Österreich: Eine retrospektive Analyse von Serumuntersuchungen aus den Jahren 2008 bis 2012 Human Toxocara-Infection in Austria: A retrospective study on serum analysis between 2008 and 2012

A Phase IIIb/IV Randomized, Controlled, Double-blind, Double-dummy, Parallel Group Study to Compare the Efficacy of Fidaxomicin to Vancomycin in the Sustained Clinical Cure of Clostridium Difficile Infection in Adults Receiving Immunosuppressive Therapy. A perioperative, single-arm multicentre Phase II academic trial to investigate the efficacy and safety of Panitumumab in combination with Irinotecan/5-Fluorouracil/Leucovorin (FOLFIRI) in patients with previously untreated, wild-type KRAS, potentially resectable colorectal cancer liver metastases. A multicentre, randomised, double-blind, parallel group study comparing the efficacy and safety of inhaled salmeterol xinafoate 50mcg bd with that of salbutamol 200mcg to use “as required” from Diskhalers for twelve months in children with asthma. A 9-Week, Randomized, Double-Blind, Placebo-Controlled, Flexible-Dosage (up to 425 mg/day), Parallel-Group Study to Evaluate the Efficacy and Safety of Modafinil (Film-Coated Tablet) in Children with Attention-Deficit/Hyperactivity Disorder. A double-blind, parallel group, study to compare the efficacy and safety of piracetam with placebo in children with specific learning disabilities.

A phase II study comparing the efficacy and pharmacokinetic/pharmacodynamic profile of acetaminophen extended release suspension, acetaminophen extended release chewable tablets, and acetaminophen elixir in febrile children. Jun 1997.A phase II study comparing the efficacy and pharmacokinetic/pharmacodynamic profile of acetaminophen extended release suspension, acetaminophen extended release chewable tablets, and acetaminophen elixir in febrile children. Jun 1997. A comparison of the efficacy and safety of ibuprofen suspension dosed at 5 mg/kg and 10 mg/kg and acetaminophen elixir dosed at 12.5 mg/kg to placebo in children with sore throat pain.

Evaluation of the results of a study in children with unprogressive syndromes of CNS disturbances and simultaneous retarded mental development, treated with Nootropil. To determine the safety and efficacy of Alupent Syrup administered to children.

urologe graz dr baumgartner gerd

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