Latest Trials

EudraCT Number: 2006-006912-31

Sponsor Protocol Number: AMV-12_12_2006

Start Date:

Sponsor Name: Universitätsklinikum Schleswig-Holstein

Full Title: Vereidung maschineller Beatmung bei sehr kleinen Frühgeborenen - Avoid mechanical ventilation (The AMV-Trial)

Medical condition: Respiratory distress syndrom of preterm infants (ICD 10: P22.0)

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Preterm newborn infants, Under 18

Gender: Male, Female

Trial protocol: DE (Ongoing)

Trial results: (No results available)

EudraCT Number: 2020-000412-30

Sponsor Protocol Number: LF111/401

Start Date:

Sponsor Name: Chemo Research S.L.

Full Title: A multicenter, open-label, controlled study to investigate the effect of either LF111 or Drospirenone chewable tablets on bone mineral density (BMD) in adolescent and adult women in comparison with...

Medical condition: Oral contraception

Disease:	Version	SOC Term	Classification Code	Term	Level
	21.0	10022891 - Investigations	10049470	Bone density decreased	PT

Population Age: Adolescents, Under 18, Adults

Gender: Female

Trial protocol: CZ (Ongoing) PL (Ongoing)

Trial results: (No results available)

EudraCT Number: 2019-000205-77

Sponsor Protocol Number: KF5503-75

Start Date:

Sponsor Name: Grünenthal GmbH

Full Title: Open-label investigation of the pharmacokinetic profile, safety, tolerability, and efficacy of multiple administrations of tapentadol oral solution used for treatment of acute pain in children aged...

Medical condition: Moderate to severe acute pain

Disease:	Version	SOC Term	Classification Code	Term	Level
	20.1	100000004867	10066714	Acute pain	LLT

Population Age: Children, Under 18

Gender: Male, Female

Trial protocol: PL (Completed)

Trial results: View results

EudraCT Number: 2020-002046-16

Sponsor Protocol Number: MARS_2020

Start Date:

Sponsor Name: Fakultní nemocnice Brno

Full Title: A Randomised, double-blinded, placebo-controlled, multicenter study of efficacy, safety and side effects of highly diluted atropine collyrium in slowing the progression of myopia (shortsightedness)...

Medical condition: Myopia in children

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: CZ (Ongoing)

Trial results: (No results available)

EudraCT Number: 2017-003643-38

Sponsor Protocol Number: 17-HPNCL-01

Start Date:

Sponsor Name: Fondation Lenval - Hôpitaux Pédiatriques de Nice CHU-LENVAL

Full Title: INTRANASAL KETAMINE IN THE REDUCTION OF THE ISOLATED FRACTURES OF THE HIGHER MEMBER OF THE CHILD TO PEDIATRIC EMERGENCIES

Medical condition: a fracture isolated from the distal end of the closed upper limb, requiring a reduction

Disease:	Version	SOC Term	Classification Code	Term	Level
	20.0	10022117 - Injury, poisoning and procedural complications	10016997	Forearm fracture	PT

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: FR (Ongoing)

Trial results: (No results available)

EudraCT Number: 2017-004207-52

Sponsor Protocol Number: CQGE031C2202

Start Date:

Sponsor Name: Novartis Pharma AG

Full Title: A multicenter, randomized, double-blind, placebo-controlled phase 2b dose-finding study to investigate the efficacy and safety of ligelizumab (QGE031) in adolescent patients with Chronic Spontaneou...

Medical condition: Chronic Spontaneous Urticaria

Disease:	Version	SOC Term	Classification Code	Term	Level
	20.0	10040785 - Skin and subcutaneous tissue disorders	10072757	Chronic spontaneous urticaria	PT

Population Age: Adolescents, Under 18

Gender: Male, Female

Trial protocol: DE (Completed) ES (Completed) BE (Completed) HU (Completed) EE (Completed)

Trial results: View results

EudraCT Number: 2014-000791-26

Sponsor Protocol Number: PHRI13-GF/LEVNEONAT-1

Start Date:

Sponsor Name: CHRU TOURS

Full Title: Lévétiracétam pour le traitement en première intention des convulsions du nouveau-né : étude de phase II

Medical condition: Nouveau-nés à terme présentant des convulsions dans les premières 72h de vie. Nés dans un contexte d'asphyxie périnatale qu'ils soient éligibles ou non à l'hypothermie thérapeutique.

Disease:	Version	SOC Term	Classification Code	Term	Level
	19.0	100000004852	10070512	Hypoxic-ischemic encephalopathy	LLT

Population Age: Newborns, Under 18

Gender: Male, Female

Trial protocol: FR (Ongoing)

Trial results: (No results available)

EudraCT Number: 2008-007667-17

Sponsor Protocol Number: FINNjA-DM

Start Date:

Sponsor Name: Dekan des Fachbereichs Medizin der Johann Wolfgang Goethe-Universität Frankfurt/M.

Full Title: Doppelblinde, randomisierte Placebo-kontrollierte crossover-Studie zur Erfassung des Effektes einer DPP-IV-Hemmung auf die Zahl und Funktion von Progenitorzellen sowie die Endothelfunktion von Pati...

Medical condition: Patients with stable diabetes mellitus typ 2 and HbA1c between 7,0% and 10,0%

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: DE (Prematurely Ended)

Trial results: (No results available)

EudraCT Number: 2011-003743-22

Sponsor Protocol Number: D9422C00001

Start Date:

Sponsor Name: AstraZeneca AB

Full Title: A Multicenter, Open label, Non-Comparative Study to Evaluate the Safety of Entocort EC for the Treatment of Crohn's Disease in Paediatric Subjects Aged 5 to 17 Years, Inclusive

Medical condition: Crohn's Disease

Disease:

Version

SOC Term

Classification Code

Term

Level

Population Age: Children, Adolescents, Under 18

Gender: Male, Female

Trial protocol: DE (Completed) IT (Completed)

Trial results: View results

EudraCT Number: 2010-020437-12

Sponsor Protocol Number: DT-DP-D2b

Start Date:

Sponsor Name: DermaTools Biotech GmbH

Full Title: A multicentric, double blind, randomized, comparative Phase II b study of the efficacy of a wound healing solution in patients with diabetic foot ulcer

Medical condition: diabetic foot ulcer

Disease:	Version	SOC Term	Classification Code	Term	Level
	12.1		10012664	Diabetic foot ulcer	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended)

Trial results: (No results available)

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