Ethikkommission der Medizinischen Universität Wien

Dec 1994.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. Dec 1994. A phase III combined study of efficacy and side effects profile of extended release acetaminophen pediatric chewable tablets compared to acetaminophen eight-hour extended release pediatric suspension in the treatment of febrile children. Aug 1998.A phase III combined study of efficacy and side effects profile of extended release acetaminophen pediatric chewable tablets compared to acetaminophen eight-hour extended release pediatric suspension in the treatment of febrile children. Aug 1998.

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randomised phase to compare the safety and efficacy of Movicol and lactulose for maintenance therapy. 94-406, Unpublished Report CSR204.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.

Das GEFS+ Spektrum: Genotyp-Phänotyp-Korrelation beim Dravet-Syndrom – eine Retrospektive Datenanalyse Sprectrum of GEFS+: genotype-phenotype correlation in patients with Dravet-Syndrome – a retrospective data analysis

A phase IV, multi-centre, double-blind, randomised, parallel group study in general practice to compare the efficacy and tolerability of inhaled salmeterol xinafoate 50 micrograms bd with placebo, both administered via the Diskhaler, in the treatment of episodic asthma induced by upper respiratory tract infection (URTI) in 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. Controlled clinical study comparing the efficacy of twice daily applications of westcort (hydrocortisone valerate) cream 0,2% and Kenalog (triamcinolonacetonide) cream 0,1% in the treatment of children with atopic dermatitis.

Piracetam for the treatment of sickle cell disease in children – a double blind test. The question of correlations between biological and clinical indices in children with mental deficiency. The clinical investigation of piracetam (UCB 6215, Nootropil) in treatment of mentally delayed children with hyperactivity. Statistical report of a controlled trial of the effect of Nootropil in epileptic children.

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.

“New Therapies”- Symptom burden and experiences of patients with advenced colorectal cancer within a antiangiogenetic therapy. A qualitative study. Clinical evaluation of Duraphat varnish in the prevention of dental caries in children and in the control of cervical hypersensitivity in adults. Post-marketing surveillance trial evaluating efficacy and tolerability of a valerian root extract in 55 children.

  • Determination of the pharmacokinetics and safety of risperidone at steady state in children and adolescents 5 to less than 18 years of age.
  • A multicentre randomised controlled study.
  • Piracetam therapy does not enhance cognitive functioning in children with Down syndrome.
  • Patient satisfaction was high and serum hormone values were improved.
  • “New Therapies”- Symptom burden and experiences of patients with advenced colorectal cancer within a antiangiogenetic therapy.

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.

None of the patients who complied with post-implant procedure instructions experienced infection or pellet extrusion. Patient satisfaction was high and serum hormone values were improved.

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.

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.

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.

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