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EudraCT Number: 2004-001583-52

Sponsor Protocol Number: Intu

Start Date: 2004-09-22

Sponsor Name: Lund University Hospital

Full Title: Balanced anestesia for intubation of newborn premature infants – a randomized intervention study Balanserad anestesi för intubation av nyfödda prematura barn – en randomiserad interventionsstudie

Medical condition: Respiratory insufficiency in prematrue infants requiring ventilatory assistance and therefore intubation. Premedication before intubation.

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Preterm newborn infants, Newborns, Under 18

Gender: Male, Female

Trial protocol: SE (Completed)

Trial results: (No results available)

EudraCT Number: 2005-000393-47

Sponsor Protocol Number: SP000680

Start Date: 2004-09-22

Sponsor Name: AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA

Full Title: Effect of Cannabis Based Medicine Extract Sativex on brain function as assessed by fMRI and neurophysiologic evaluation in patients with Multiple Sclerosis a double blind, randomised, placebo-co...

Medical condition: Treatment of spasticity in patients with Multiple Sclerosis

Disease:	Version	SOC Term	Classification Code	Term	Level
	9.1		10028245	Multiple sclerosis	LLT

Population Age: Adults

Gender: Male, Female

Trial protocol: IT (Completed)

Trial results: (No results available)

EudraCT Number: 2004-002125-42

Sponsor Protocol Number: CTH9507J

Start Date: 2004-09-22

Sponsor Name: AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO"

Full Title: EFFECT OF PROLONGED TREATMENT WITH TH9507 ON IGF-I LEVELS IN ADOLESCENTS WITH ISOLATED GH DEFICIENCY DUE TO HYPOTHALAMIC PATHOGENESIS

Medical condition: EVALUATION OF GROWTH HORMONE RELEASE

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults

Gender: Male, Female

Trial protocol: IT (Ongoing)

Trial results: (No results available)

EudraCT Number: 2004-001967-24

Sponsor Protocol Number: L 9259

Start Date: 2004-09-22

Sponsor Name: Sanofi-Synthelabo Rt.

Full Title: Kiegészítő zolpidem kezelés friss antidepresszáns kezelés alatt álló disztimiás vagy depressziós betegek alvászavarának kezelésében

Medical condition: A depresszióban szenvedő betegek alvászavarára jellemzően megfigyelhető kóros alvásparaméterek lehetnek az elalvás nehezítettsége, töredezett, felszínes alvás gyakori felébredésekkel, az újra elalv...

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: HU (Completed)

Trial results: View results

EudraCT Number: 2004-001091-40

Sponsor Protocol Number: 2-47-52030-722

Start Date: 2004-09-22

Sponsor Name: Beaufour Ipsen Pharma

Full Title: A Phase III, Prospective, Multicentre, Randomised, Open, Parallel Group Comparison of Lanreotide Autogel (90 and 120mg) Administered by Deep Subcutaneous Injection Every Four Weeks, with Sandostati...

Medical condition: Treatment of clinical symptoms of carcinoid syndrome.

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FI (Completed)

Trial results: View results

EudraCT Number: 2004-000755-41

Sponsor Protocol Number: RA/PR/3301/010/03

Start Date: 2004-09-22

Sponsor Name: Chiesi Farmaceurtici S.p.A

Full Title: A three-month, double-blind, double dummy, parallel group, controlled study comparing the efficacy and safety between 12 µg twice daily of Formoterol-HFA and 12 µg twice daily of Formoterol-DPI (Fo...

Medical condition: Children Persistent Asthma

Disease:	Version	SOC Term	Classification Code	Term	Level
	7.0		10003553		Low

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: CZ (Completed)

Trial results: View results

EudraCT Number: 2007-005396-34

Sponsor Protocol Number: RG_10-040

Start Date: 2004-09-22

Sponsor Name: University of Birmingham

Full Title: Treatment Protocol for T-Cell and B-Precursor Cell Lymphoblastic Lymphoma of the European Inter-group Co-operation on Childhood Non-Hodgkin-Lymphoma (EICNHL)

Medical condition: lymphoblastic lymphoma

Disease:	Version	SOC Term	Classification Code	Term	Level
	9.1		10065923	Lymphoblastic lymphoma	LLT

Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults

Gender: Male, Female

Trial protocol: GB (Completed)

Trial results: View results

EudraCT Number: 2004-000348-25

Sponsor Protocol Number: D6160C00031

Start Date: 2004-09-22

Sponsor Name: ASTRAZENECA

Full Title: GALLANT 8 - A 24-Week Randomized, Double-Blind, Parallel-Group, Multi-Centre, Placebo-Controlled Study to Evaluate the Efficacy, Safety and Tolerability of Tesaglitazar Therapy when Added to the Th...

Medical condition: To prevent vascular disease associated with insulin resistence.

Disease:	Version	SOC Term	Classification Code	Term	Level
	9.1		10053247	Insulin-requiring type 2 diabetes mellitus	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: IT (Completed)

Trial results: View results

EudraCT Number: 2004-001033-41

Sponsor Protocol Number: H6D-MC-LVFZ

Start Date: 2004-09-22

Sponsor Name: ELI LILLY

Full Title: A Randomized, Double-Blind, Parallel-Design, Placebo-Controlled Study to Evluate the Efficacy and Safety of Tadalafil (2.5 mg e 5 mg) administered once daily to men with diabetes mellitus and erect...

Medical condition: Therapy of erectile disfunction to subjects with diabetes mellitus and erectile disfunction with a 2.5 mg or 5 mg daily dosing.

Disease:	Version	SOC Term	Classification Code	Term	Level
	6.1		10061461		PT

Population Age: Adults, Elderly

Gender: Male

Trial protocol: IT (Completed)

Trial results: (No results available)

EudraCT Number: 2004-001551-11

Sponsor Protocol Number: Iloprost

Start Date: 2004-09-22

Sponsor Name: Lund University Hospital

Full Title: Behandling av förhöjt pulmonellt arteriellt tryck med inhalerad iloprost

Medical condition: Nyfödda barn som är i behov av respiratorvård pga RDS, mekoniumaspiration eller primär lunghypertension

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Preterm newborn infants, Newborns, Under 18

Gender: Male, Female

Trial protocol: SE (Ongoing)

Trial results: (No results available)

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