- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
25 result(s) found for: Perturbation.
Displaying page 1 of 2.
EudraCT Number: 2009-018191-34 | Sponsor Protocol Number: FOL003 | Start Date*: 2010-07-21 | |||||||||||
Sponsor Name:Follica Inc. | |||||||||||||
Full Title: A Study to Explore the Effect of Controlled Cutaneous Perturbation and Pharmacologic Modulation for Inducing Follicular Neogenesis | |||||||||||||
Medical condition: Male subjects with androgenetic alopecia | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001031-22 | Sponsor Protocol Number: CCR2749 | Start Date*: 2007-12-18 |
Sponsor Name:Institute of Cancer Research | ||
Full Title: The Potentiation of Efficacy of Radiotherapy in Non-Small-Cell Lung Cancer (NSCLC) by Inhibition of Akt Activation | ||
Medical condition: Non-small-cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002791-33 | Sponsor Protocol Number: 2007-17 | Start Date*: 2008-04-16 |
Sponsor Name:Assistance Publique Hopitaux de marseille | ||
Full Title: Effet aigu d’une insulinothérapie intensive sur le métabolisme des lipoparticules riches en triglycérides (LRT) intestinales chez le patient diabétique de type 2 | ||
Medical condition: DIABETIQUE DE TYPE II | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002208-40 | Sponsor Protocol Number: 65/2005/U/Sper | Start Date*: 2005-06-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Levetiracetam Keppra in the dyskinesias induced from levodopa in patients with disease of Parkinson. Clinical study pilot in open, with farmacokinetic-farmacodynamic monitoring of the effects. | |||||||||||||
Medical condition: Treatment of the induced coreiche dyskinesias from the therapy with levodopa in patients with Disease of Parkinson. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013476-53 | Sponsor Protocol Number: PHRC-N/2009/POK-01 | Start Date*: 2010-09-02 |
Sponsor Name:CHU de Nîmes | ||
Full Title: Evaluation des performances de l’imagerie cérébrale isotopique du métabolisme glucidique en TEP (18F-FDG) et de la perfusion en TEMP (99mTc-ECD) pour le diagnostic de maladie d’Alzheimer au stade p... | ||
Medical condition: Maladie d'alzheimer au stade prodromal | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001835-36 | Sponsor Protocol Number: 68923 | Start Date*: 2008-07-09 | |||||||||||
Sponsor Name:Gedeon Richter Plc. | |||||||||||||
Full Title: Single center, exploratoric, open-label study to investigate the add-on effect of vinpocetin to the haemorheological effect of 100 mg acetyl-salicylicum in patients with chronic cerebrovascular dis... | |||||||||||||
Medical condition: Aspirin resistance in patients with chronic cerebrovascular disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000885-39 | Sponsor Protocol Number: 02289 | Start Date*: 2021-01-12 | |||||||||||
Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
Full Title: Safety and Efficacy of Induced Pluripotent Stem Cell-derived Engineered Human Myocardium as Biological Ventricular Assist Tissue in Terminal Heart Failure | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019285-86 | Sponsor Protocol Number: EB79 | Start Date*: 2010-05-07 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Emotional Brain | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A single blind, randomized, cross-over placebo controlled dose finding study to investigate the pharmacokinetic profile of 3 doses of sublingual testosterone solution and their effect on physiologi... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: This pharmacokinetic trial will be conducted in healthy women, but it is a part of a developmental program for medicine for Hypoactive Sexual Desire Disorder (comorbidity with other sexual dysfunct... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000202-20 | Sponsor Protocol Number: RC-P0041 | Start Date*: 2015-06-22 | |||||||||||||||||||||||||||||||
Sponsor Name:Groupement des Hôpitaux de l’Institut Catholique de Lille (GHICL) | |||||||||||||||||||||||||||||||||
Full Title: Effect and tolerance of ketamine's subcutaneous bolus during painful care, refractory of bedsore, ulcer, vascular wound care in palliative care units. | |||||||||||||||||||||||||||||||||
Medical condition: Patients’ palliative care for bedsores, ulcers or vascular wounds, which are general characteristics of the patient population that will be included: usually elderly, undernourished and of multiple... | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019540-39 | Sponsor Protocol Number: EB80 | Start Date*: 2010-05-12 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Emotional Brain | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A double blind, randomized, cross-over placebo controlled study to investigate the efficacy of sublingual testosterone solution on physiological and subjective arousal in healthy, sexually dysfunct... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: This pharmacodynamic trial will be conducted in sexually dysfunctional otherwise healthy women, but it is a part of a developmental program for medicine for Hypoactive Sexual Desire Disorder (comor... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023648-34 | Sponsor Protocol Number: HT-ANAM-301 | Start Date*: 2011-09-15 | ||||||||||||||||
Sponsor Name:Helsinn Therapeutics (U.S.), Inc. | ||||||||||||||||||
Full Title: Anamorelin HCl in the Treatment of Non-Small Cell Lung Cancer – Cachexia (NSCLC-C): A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study to Evaluate the Safety and Efficacy ... | ||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer related Cachexia (NSCLC-C) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) NL (Completed) ES (Completed) DE (Completed) CZ (Completed) IT (Completed) SI (Completed) HU (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011774-15 | Sponsor Protocol Number: BASt01 | Start Date*: 2009-07-15 | |||||||||||||||||||||
Sponsor Name:Federal Highway Research Institute / Bundesanstalt für Straßenwesen (BASt) | |||||||||||||||||||||||
Full Title: Effects of opioid analgesics on driving ability of pain patients [Untersuchung zur Fahrsicherheit von Schmerzpatienten] | |||||||||||||||||||||||
Medical condition: patients suffering from chronic non-cancer pain responsive to opioid analgesics under already existing long-term treatment | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008377-56 | Sponsor Protocol Number: 2008-249 | Start Date*: 2009-03-10 | |||||||||||||||||||||||||||||||
Sponsor Name:Palliativ medicinsk afdeling, Bispebjerg Hospital | |||||||||||||||||||||||||||||||||
Full Title: Melatonin for træthed og andre symptomer hos patienter med fremskreden kræft | |||||||||||||||||||||||||||||||||
Medical condition: Træthed og andre symptomer hos patienter med freskreden kræft i palliativ fase | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-023649-31 | Sponsor Protocol Number: HT-ANAM-302 | Start Date*: 2011-07-29 | ||||||||||||||||
Sponsor Name:Helsinn Therapeutics (U.S.), Inc. | ||||||||||||||||||
Full Title: Anamorelin HCl in the Treatment of Non-Small Cell Lung Cancer – Cachexia (NSCLC-C): A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase III Study to Evaluate the Safety and Efficacy ... | ||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer related Cachexia (NSCLC-C) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) GB (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000464-27 | Sponsor Protocol Number: ART27.13-100 | Start Date*: 2020-10-29 | |||||||||||
Sponsor Name:Artelo Biosciences Limited | |||||||||||||
Full Title: A Phase 1/2 Trial of the Synthetic Cannabinoid ART27.13 in Patients with Cancer Anorexia and Weight Loss | |||||||||||||
Medical condition: Cancer anorexia and weight loss | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Trial now transitioned) NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005749-18 | Sponsor Protocol Number: B01-02 | Start Date*: 2013-08-29 | |||||||||||||||||||||
Sponsor Name:Athersys, Inc | |||||||||||||||||||||||
Full Title: Double-Blind, Randomized, Placebo-Controlled, Phase 2 Safety and Efficacy Trial of MultiStem® in Adults With Ischemic Stroke | |||||||||||||||||||||||
Medical condition: acute ischemic stroke | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001916-37 | Sponsor Protocol Number: MATRICS_WP6-1 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:RADBOUD UNIVERSITY MEDICAL CENTER | |||||||||||||
Full Title: The neuropsychological characterization of aggressive behaviour in children and adolescents with Conduct Disorder or Oppositional Defiant Disorder (CD/ODD) | |||||||||||||
Medical condition: Aggressive behavior in children and adolescents with Conduct Disorder (CD) or Oppositional Defiant Disorder (ODD) | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002318-15 | Sponsor Protocol Number: 010921 | Start Date*: 2021-09-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Copenhagen University Hospital, Amager and Hvidovre, Department of Clinical Research | ||||||||||||||||||||||||||||||||||||||
Full Title: A pharmacological trial with Sativex® and gentamicin for optimized pharmacological treatment of older patients with a focus on appetite stimulation and renal risk drugs | ||||||||||||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024425-20 | Sponsor Protocol Number: Esperanz-002 | Start Date*: 2011-03-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Leiden University Medical Centre | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase III Randomized Double-blind Cross-over trial of Supersaturated Calcium-phosphate rinse (Caphosol®) versus NaCl 0.9% in the relief of Oral Mucositis in renal cell carcinoma, hepatocellular car... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: oral mucositis in renal cell carcinoma, hepatocellular carcinoma, and gastrointestinal stromal tumor | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003543-30 | Sponsor Protocol Number: EB93 | Start Date*: 2012-08-24 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Emotional Brain BV | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A double-blind, randomized, placebo-controlled, proof of concept study to investigate the differences between the combined administration of 0.5 mg sublingual testosterone and 10 mg buspirone and 1... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Hypoactive Sexual Desire Disorder Sexual Interest/Arousal Disorder | ||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
