- Trials with a EudraCT protocol (1,769)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,769 result(s) found for: Quality of Life (QOL).
Displaying page 1 of 89.
EudraCT Number: 2005-002484-87 | Sponsor Protocol Number: GAST-TaxXel | Start Date*: 2005-07-11 |
Sponsor Name:Raija Ristamäki | ||
Full Title: Biweekly Taxotere in combination with Xeloda as first-line treatment in patients with advanced gastric cancer | ||
Medical condition: advanced gastric cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004835-72 | Sponsor Protocol Number: UB-MedSci-001/2004 | Start Date*: 2005-01-12 |
Sponsor Name:University of Birmingham [...] | ||
Full Title: A study to determine the effects of growth hormone (GH) replacement therapy on quality of life and cardiovascualr risk in GH deficient adults | ||
Medical condition: Growth hormone deficiency in adult life | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-005424-97 | Sponsor Protocol Number: CIGE025EFR02 | Start Date*: 2015-01-28 | |||||||||||
Sponsor Name:NOVARTIS PHARMA SAS | |||||||||||||
Full Title: A phase IV, multicenter, single-arm and open-label study to explore the impact on quality of life of omalizumab (Xolair®) in patients with chronic spontaneous urticaria (CSU) who remain symptomatic... | |||||||||||||
Medical condition: chronic spontaneous urticaria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001023-39 | Sponsor Protocol Number: ML28786 | Start Date*: 2013-08-08 | |||||||||||
Sponsor Name:Roche Austria GmbH | |||||||||||||
Full Title: LISAH: AN OPEN-LABEL, RANDOMISED PHASE II STUDY ASSESSING QUALITY OF LIFE ASSOCIATED WITH SUBCUTANEOUS TRASTUZUMAB INJECTED INTO THE THIGH OR UPPER ARM IN PATIENTS WITH HER2-POSITIVE EARLY BREAST C... | |||||||||||||
Medical condition: HER2-positive early breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: AT (Temporarily Halted) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000547-34 | Sponsor Protocol Number: QoL-ESC RevMDS | Start Date*: 2008-06-09 | |||||||||||
Sponsor Name:ASSOCIAZIONE QOL-ONE | |||||||||||||
Full Title: Lenalidomide for Myelodysplastic Syndromes: Efficacy, Safety, Cardiac Changes, and Quality of Life (QoL-ESC RevMDS) | |||||||||||||
Medical condition: Low or Intermediate-1 IPSS risk MDS with del(5q)as a single or combined cytogenetic abnormality and with anemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003028-59 | Sponsor Protocol Number: NL62684.091.17 | Start Date*: 2018-06-06 |
Sponsor Name:Radboud University Medical Centre | ||
Full Title: Treatment with Recombinant human Interleukin 1 receptor antagonist (Anakinra) in patients with Anaplastic Thyroid Cancer: a proof of concept study | ||
Medical condition: Anaplastic Thyroid Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005362-19 | Sponsor Protocol Number: TAVAB | Start Date*: 2014-07-17 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Therapy of antibody-mediated autoimmune diseases by Bortezomib (TAVAB) | ||
Medical condition: Myasthenia Gravis Systemic Lupus Erythematosus Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-000497-28 | Sponsor Protocol Number: PTC923-MD-004-PKU | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:PTC Therapeutics, Inc. | |||||||||||||
Full Title: Phase 3 Open-Label Study of PTC923 (Sepiapterin) in Phenylketonuria | |||||||||||||
Medical condition: Metabolic Disorders - Phenylketonuria | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) DK (Trial now transitioned) NL (Trial now transitioned) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002665-30 | Sponsor Protocol Number: RENAISSANCE | Start Date*: 2016-01-11 |
Sponsor Name:Krankenhaus Nordwest gGmbH | ||
Full Title: Effect of chemotherapy alone vs. chemotherapy followed by surgical resection on survival and quality of life in patients with limited-metastatic adenocarcinoma of the stomach or esophagogastric jun... | ||
Medical condition: limited-metastatic adenocarcinoma of the stomach or esophagogastric junction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002096-96 | Sponsor Protocol Number: NL57849.068.16 | Start Date*: 2016-09-20 |
Sponsor Name:Maastricht University Medical Center | ||
Full Title: TOPical Imiquimod treatment of high-grade Cervical intraepithelial neoplasia, a multicenter, open-label, non-randomized, controlled study (TOPIC-3 study) | ||
Medical condition: High-grade Cervical Intraepithelial Neoplasia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005127-27 | Sponsor Protocol Number: CIGE025ENL01T | Start Date*: 2015-05-29 |
Sponsor Name:UMC Utrecht | ||
Full Title: Markers of Efficacy of Xolair (Omalizumab) in Chronic Spontaneous Urticaria | ||
Medical condition: Chronic spontaneous urticaria | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004101-75 | Sponsor Protocol Number: S56122-ML10190 | Start Date*: 2014-03-28 | ||||||||||||||||
Sponsor Name:UZ Leuven | ||||||||||||||||||
Full Title: Randomized crossover trial to assess the effects and quality of life in patients with locally advanced or metastatic pancreatic cancer treated with gemcitabine in combination with nab-paclitaxel: Q... | ||||||||||||||||||
Medical condition: locally advanced or metastatic pancreatic cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015059-26 | Sponsor Protocol Number: 510460 | Start Date*: 2010-08-19 |
Sponsor Name:Actavis GmbH & Co. KG | ||
Full Title: Efficacy of 12 weeks oral Pentalong® on Exercise Capacity and Quality of Life in Patients With Systolic Heart Failure and Secondary Pulmonary Hypertension Short title: CAESAR Clinical efficacy ... | ||
Medical condition: Woman and men suffering from heart failure NYHA II-IV and secondary pulmonary hypertension Objectives PVR improvement after a 12 week oral Pentalong® therapy in addition to standard long-term HF... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003068-47 | Sponsor Protocol Number: UROBOTOX 1 | Start Date*: 2005-09-22 |
Sponsor Name:Region Skåne, Universitetssjukhuset i Lund, Urologiska kliniken | ||
Full Title: Behandling med botulinumtoxin vid neurogen blåsfunktionsstörning | ||
Medical condition: The trial addresses patients with severe symptoms of neurogenic detrusor overactivity (urgency and/or urge incontinence). Eligible are those patients who have failed conservative treatment such as ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002550-20 | Sponsor Protocol Number: AMIRA | Start Date*: 2017-07-17 |
Sponsor Name:University of Ulm | ||
Full Title: Allogeneic microbiota-reconstitution (AMR) for the Treatment of patients with diarrhea-predominant irritable bowel Syndrome (IBS-D) - the AMIRA trial | ||
Medical condition: diarrhea-predominant irritable bowel syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000739-97 | Sponsor Protocol Number: HIC | Start Date*: 2011-05-05 |
Sponsor Name:Med. Univ. Wien | ||
Full Title: Prospective, randomized, controlled, open-label study evaluating quality of life in patients with advanced malignant tumors with and without “add-on” homeopathy | ||
Medical condition: Homeopathic remedies as add on therapie in cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000959-15 | Sponsor Protocol Number: HOE901/4057 | Start Date*: 2005-05-17 |
Sponsor Name:sanofi-aventis | ||
Full Title: A multicenter clinical trial to evaluate quality of life in patients with Type 2 diabetes before and after changing therapy to a combination of insulin glargine and oral antidiabetic drugs in a rea... | ||
Medical condition: Patients with Type 2 diabetes inadequately controlled on a combination of highest tolerable dose of oral antidiabetic drugs (OAD) + neutral protamine hagedorn (NPH) insulin for more than 3 months | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003536-12 | Sponsor Protocol Number: CIGE025B1301E1 | Start Date*: 2016-02-16 |
Sponsor Name:Novartis Pharmaceuticals | ||
Full Title: An Extension Study to CIGE025B1301 to Evaluate the Long-term Safety, Tolerability and Efficacy of Omalizumab in Japanese Children (6 - 15 Years) With Inadequately Controlled Allergic Asthma Despite... | ||
Medical condition: Allergic Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2022-001909-53 | Sponsor Protocol Number: MW2012-01-01.BExt | Start Date*: 2022-10-24 |
Sponsor Name:MediWound Ltd. | ||
Full Title: Long Term (>30 months following wound closure) assessments of cosmesis, function and quality of life in pediatric subjects following participation in study MW2012-01-01 evaluating the efficacy and ... | ||
Medical condition: To evaluate and compare the cosmesis, function and QoL in children who had their target burn wounds eschar removed by NexoBrid or by SOC in study MW2012-01-01 | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000292-83 | Sponsor Protocol Number: Tallisur | Start Date*: 2017-08-30 |
Sponsor Name:Servier Deutschland GmbH | ||
Full Title: Prospective, Multicenter, Open-label Phase IV trial of Trifluridine/Tipiracil to Evaluate the Health-related Quality of Life in Patients with Metastatic Colorectal Cancer | ||
Medical condition: Histologically or cytologically confirmed UICC stage IV carcinoma of colon or rectum with metastasis (metastatic colorectal cancer) with need for treatment due to progression | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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