Clinical trials for placebo

The European Union Clinical Trials Register allows you to search for protocol and results information on:

interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC

clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
Clinical Trials Information System (CTIS).

The EU Clinical Trials Register currently displays 44334 clinical trials with a EudraCT protocol, of which 7366 are clinical trials conducted with subjects less than 18 years old. The register also displays information on 18700 older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).

Examples: Cancer AND drug name. Pneumonia AND sponsor name.
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Trials with a EudraCT protocol (12,687)
Paediatric studies in scope of Art45 of the Paediatric Regulation (1,156)

12,687 result(s) found for: placebo. Displaying page 458 of 635.

EudraCT Number: 2012-003213-34

Sponsor Protocol Number: CH2012-001

Start Date*: 2012-11-13

Sponsor Name:ISTITUTO CLINICO HUMANITAS

Full Title: MEthylprednisoloneNacinHepatIcResections “MENHIR”

Medical condition: patients candidate to liver resection

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	10019805 - Hepatobiliary disorders	10019805	Hepatobiliary disorders	SOC

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: IT (Ongoing)

Trial results: (No results available)

EudraCT Number: 2011-000602-22

Sponsor Protocol Number: B2611002

Start Date*: 2011-06-29

Sponsor Name:Pfizer Inc

Full Title: A 12-WEEK, PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, DOSE-RANGING, PARALLEL GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ONCE DAILY PF-04991532 AND SITAGLIPTIN IN ADULT PATIENTS ...

Medical condition: Type 2 Diabetes Mellitus

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	13.1	10027433 - Metabolism and nutrition disorders	10045242	Type II diabetes mellitus	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: SK (Completed) HU (Completed)

Trial results: View results

EudraCT Number: 2012-000298-22

Sponsor Protocol Number: PRENECAL

Start Date*: 2012-12-05

Sponsor Name:Fundació Clínic per a la Recerca Biomèdica

Full Title: Study to assess the efficacy and safety of oral potassium citrate on the Prevention of nephrocalcinosis in extreme premature: a clinical trial, randomized, double-blind placebo controlled trial. St...

Medical condition: incidence of nephrocalcinosis in extremely preterm infants

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	10038359 - Renal and urinary disorders	10029146	Nephrocalcinosis	PT

Population Age: Preterm newborn infants, Under 18

Gender: Male, Female

Trial protocol: ES (Completed)

Trial results: (No results available)

EudraCT Number: 2013-003016-45	Sponsor Protocol Number: APCP-112	Start Date*: 2013-09-11
Sponsor Name:Araim Pharmaceuticals
Full Title: A double blind, placebo controlled Phase 2 dose ranging study of the effects of ARA 290 on corneal nerve fiber density and neuropathic symptoms of patients with sarcoidosis
Medical condition: small fiber neuropathy
Disease:
Population Age: Adults, Elderly		Gender: Male, Female
Trial protocol: NL (Completed)
Trial results: View results

EudraCT Number: 2013-003323-11

Sponsor Protocol Number: ITIBU001

Start Date*: 2014-10-01

Sponsor Name:"Sapienza" University of Rome

Full Title: RANDOMIZED CLINICAL TRIAL, PLACEBO-CONTROLLED, SPLIT-MOUTH, A DOUBLE-BLIND, FOR THE EVALUATION OF THE EFFECTIVENESS OF PREemptive ANALGESIA BY ADMINISTRATION OF IBUPROFEN 400MG, FOR THE CONTROL ...

Medical condition: POST-OPERATIVE ACUTE PAIN (DAPO)

Disease:	Version	SOC Term	Classification Code	Term	Level
	17.1	10017947 - Gastrointestinal disorders	10031009	Oral pain	PT
	17.1	10017947 - Gastrointestinal disorders	10030973	Oral discomfort	PT

Population Age: Adults

Gender: Male, Female

Trial protocol: IT (Ongoing)

Trial results: (No results available)

EudraCT Number: 2012-004900-37	Sponsor Protocol Number: DC05/RUP/I/13	Start Date*: 2012-11-20
Sponsor Name:J. Uriach y Compañía, S.A.
Full Title: A Phase I, Randomised, Double-blind, Placebo-controlled, Parallel group study to assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of oral Rupatadine in Healthy Japanese Subjec...
Medical condition: This is a Phase I study in helathy subjects. No condition is being treated. The IMP is approved for symptomatic treatment of allergic rhinitis and urticaria in adults and adolescents (over 12 yea...
Disease:
Population Age: Adults		Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: (No results available)

EudraCT Number: 2009-014437-24

Sponsor Protocol Number: P090203

Start Date*: 2009-09-23

Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)

Full Title: Essai randomisé d'immunonutrition par L-arginine guidée en réanimation non chirurgicale

Medical condition: Patients de réanimation non chirurgicale sous ventilation artificielle, non immunodéprimés

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	8.1		10062733	Nutritional supplement	PT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: FR (Ongoing)

Trial results: (No results available)

EudraCT Number: 2009-013763-19

Sponsor Protocol Number: CQAB149BIT01

Start Date*: 2009-09-24

Sponsor Name:NOVARTIS FARMA

Full Title: Multicenter, randomized, blinded, placebo controlled, cross over, single dose study to assess the effect of indacaterol (150 �g) versus tiotropium (18 �g) on Inspiratory Capacity in moderate COPD p...

Medical condition: moderate COPD

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	12.0		10029978	Obstructive chronic bronchitis with acute exacerbation	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: IT (Completed)

Trial results: View results

EudraCT Number: 2008-007789-51

Sponsor Protocol Number: B1971005(6108A1-2001-WW)

Start Date*: 2009-03-23

Sponsor Name:Pfizer Inc

Full Title: A Randomized, Single-Blind, Placebo-Controlled, Phase 2 Trial of the Safety, Immunogenicity, and Tolerability of Meningococcal Serogroup B (MnB) rLP2086 Vaccine at Doses of 60 µg, 120 µg, and 200 µ...

Medical condition: The test is a vaccine. The subjects are healthy adolescents.

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	10021881 - Infections and infestations	10027202	Meningitis bacterial	PT

Population Age: Children, Adolescents, Under 18, Adults

Gender: Male, Female

Trial protocol: PL (Completed) ES (Completed) Outside EU/EEA

Trial results: View results

EudraCT Number: 2006-002837-19

Sponsor Protocol Number: RD-5103-037-05

Start Date*: 2007-04-16

Sponsor Name:DERBY HOSPITALS NHS FOUNDATION TRUST

Full Title: A DOUBLE BLIND PLACEBO CONTROLLED TRIAL OF TERLIPRESSIN IN THE MANAGEMENT OF SEVERE ALCOHOLIC HEPATITIS – A PRELIMINARY STUDY

Medical condition: Severe alcoholic hepatitis as judged by a Maddrey score >32

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	8.1		10001624	Alcoholic hepatitis	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: GB (Prematurely Ended)

Trial results: View results

EudraCT Number: 2009-017468-18

Sponsor Protocol Number: CS/IV-RMF-01

Start Date*: 2010-07-02

Sponsor Name:Bioibérica S.A.

Full Title: Ensayo clínico aleatorizado, doble ciego, controlado con placebo para valorar el efecto de condroitín sulfato sobre el dolor en pacientes afectos de artrosis de rodilla mediante Resonancia Magnétic...

Medical condition: Knee osteoarthritis

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	12.1		10023476	Knee osteoarthritis	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: ES (Completed)

Trial results: (No results available)

EudraCT Number: 2009-010727-91

Sponsor Protocol Number: 00695

Start Date*: 2011-03-01

Sponsor Name:LMU München, Campus Großhadern

Full Title: Colesevelam for the treatment of bile acid malabsorption in patients with Crohn’s disease (Colesevelam für die Therapie der Gallensäuren-Malabsorption bei M. Crohn-Patienten)

Medical condition: Morbus Crohn

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	10017947 - Gastrointestinal disorders	10011401	Crohn's disease	PT

Population Age: Adults

Gender: Male, Female

Trial protocol: DE (Prematurely Ended)

Trial results: (No results available)

EudraCT Number: 2007-003343-74

Sponsor Protocol Number: PDS234

Start Date*: 2007-10-30

Sponsor Name:Academic Medical Center

Full Title: A methodological investigation to test acute changes in female sexual desire in healthy volunteersand pre- and postmenopausal women diagnosed with hypoactive sexual desiredisordersusing explicit me...

Medical condition: hypoactive sexual desire disorder in women (HSDD)

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	9.1		10062641	Female sexual arousal disorder	LLT

Population Age: Adults

Gender: Female

Trial protocol: NL (Ongoing)

Trial results: (No results available)

EudraCT Number: 2007-001841-16

Sponsor Protocol Number: VOCARE-07-01

Start Date*: 2008-09-17

Sponsor Name:Melchor Riera Jaume

Full Title: ENSAYO CLÍNICO ALEATORIZADO Y CONTROLADO DE VORICONAZOL FRENTE A PLACEBO EN LA PROFILAXIS DE ASPERGILOSIS PULMONAR EN PACIENTES COLONIZADOS CON PATOLOGÍA RESPIRATORIA CRÓNICA (ESTUDIO VOCARE)

Medical condition: Aspergilosis pulmonar invasiva

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	9.1		10022881	Invasive bronchopulmonary aspergillosis	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: ES (Ongoing)

Trial results: (No results available)

EudraCT Number: 2013-000122-60	Sponsor Protocol Number: 1.0	Start Date*: 2013-05-17
Sponsor Name:Karolinska University Hospital, Division of Pediatrics/Astrid Lindgren Children´s Hospital
Full Title: The effect of dexmedetomidine as an adjuvant to local anaesthetics for ilioinguinal blocks in paediatric patients
Medical condition: Pediatric patients receive ilioinguinal-iliohypogastric nerve blockade with 0.2ml/kg ropivacaine 0.197% and 0.3µg/kg dexmedetomidine or 0.2ml/kg ropivacaine 0.197% and saline as a placebo. Aim of t...
Disease:
Population Age: Infants and toddlers, Children, Under 18		Gender: Male, Female
Trial protocol: SE (Ongoing)
Trial results: (No results available)

EudraCT Number: 2011-003544-42

Sponsor Protocol Number: 2011-3

Start Date*: 2012-02-16

Sponsor Name:Department of Neurosurgery, PMU

Full Title: DRES - A prospective, multi-center, double blind, randomized, placebo controlled study to assess the efficacy of Dexamethason in reducing the reoperation rate in patients with chronic subdural hema...

Medical condition: operated chronic subdural hematoma

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	18.0	100000004863	10049163	Chronic subdural hematoma	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: AT (Ongoing)

Trial results: (No results available)

EudraCT Number: 2010-019768-35

Sponsor Protocol Number: ITB2010

Start Date*: 2012-07-27

Sponsor Name:

Full Title: Intrathecal baclofen treatment in dystonic cerebral palsy: a randomized clinical trial

Medical condition: dytonic cerebral palsy

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	19.1	10010331 - Congenital, familial and genetic disorders	10008129	Cerebral palsy	PT

Population Age: Children, Adolescents, Under 18, Adults

Gender: Male, Female

Trial protocol: NL (Ongoing)

Trial results: (No results available)

EudraCT Number: 2008-000281-23

Sponsor Protocol Number: Oxford University(None)

Start Date*: 2009-09-10

Sponsor Name:University of Oxford

Full Title: Melatonin in Acute Mania Investigation (MIAMI-UK)

Medical condition: Bipolar Disorder (mania and hypomania)

Disease:	Version	SOC Term	Classification Code	Term	Level
	12		10000852	Acute Mania	LLT
	12		10021030	Hypomania	LLT

Population Age: Adults

Gender: Male, Female

Trial protocol: GB (Completed)

Trial results: View results

EudraCT Number: 2012-000942-36

Sponsor Protocol Number: POWAR

Start Date*: 2012-10-22

Sponsor Name:Guys and St Thomas NHS Foundation Trust

Full Title: Are phrophylactic antibiotics necessary before laparoscopic living kidney donation? A double blind, randomised, controlled trial.

Medical condition: Post-operative infections

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	100000004862	10059428	Postoperative infection	LLT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: GB (Completed)

Trial results: View results

EudraCT Number: 2012-002840-26

Sponsor Protocol Number: PD0005

Start Date*: 2013-03-05

Sponsor Name:UCB Biosciences GmbH

Full Title: A Multicenter, Multinational, Double-blind, Placebo-controlled, 3-arm Phase 4 Study to Evaluate the Efficacy of Rotigotine on Parkinson's Disease- Associated Apathy, Motor Symptoms, and Mood

Medical condition: Parkinson's disease

Disease:	Version	SOC Term	Classification Code	Term	Level
Disease:	14.1	10029205 - Nervous system disorders	10061536	Parkinson's disease	PT

Population Age: Adults, Elderly

Gender: Male, Female

Trial protocol: AT (Completed) ES (Completed) HU (Completed) IT (Completed) BG (Completed) SI (Completed) RO (Completed) SK (Completed)

Trial results: View results

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The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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