- Trials with a EudraCT protocol (1,777)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,777 result(s) found for: Quality of Life (QOL).
Displaying page 2 of 89.
EudraCT Number: 2006-001902-10 | Sponsor Protocol Number: 2006/168 | Start Date*: 2006-05-31 |
Sponsor Name:Kirurgisk Forskningsafsnit, Herning Sygehus | ||
Full Title: Effects of caffeine on people suffering from intermittens claudication. Three double blinded, placebo-controlled cross-over studies and a follow-up study. | ||
Medical condition: Intermittens claudication, peripheral arterial disease (PAD) Atherosclerotic disease of the lower extremities | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000179-18 | Sponsor Protocol Number: RG_13-322 | Start Date*: 2015-04-28 |
Sponsor Name:University of Birmingham [...] | ||
Full Title: Local Oestrogen Treatment in Postmenopausal Women Undergoing Pelvic Organ Prolapse Surgery (LOTUS) - Feasibility Study | ||
Medical condition: Pelvic organ prolapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003506-27 | Sponsor Protocol Number: BILA-3312/PED | Start Date*: 2013-01-25 |
Sponsor Name:FAES FARMA, S.A. | ||
Full Title: A multicenter, double-blind, randomized, placebo-controlled, parallel group study to evaluate the safety and tolerability of 10 mg once daily bilastine in children from 2 to 11 years of age with e... | ||
Medical condition: Allergic Rhinoconjunctivitis and Chronic Urticaria | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Completed) ES (Ongoing) PT (Completed) PL (Completed) HR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001639-23 | Sponsor Protocol Number: VIT-2763-THAL-203 | Start Date*: 2021-10-27 | |||||||||||
Sponsor Name:VIFOR (INTERNATIONAL) INC. | |||||||||||||
Full Title: A Phase 2b, double-blind, randomised, placebo-controlled, multicentre study to assess the efficacy and safety of VIT-2763 multiple doses in adults with transfusion-dependent ß-thalassaemia | |||||||||||||
Medical condition: transfusiondependent ß-thalassaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) BG (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004043-23 | Sponsor Protocol Number: CoFu-01 | Start Date*: 2020-07-23 | |||||||||||
Sponsor Name:University Hospital Schleswig-Holstein (UKSH) | |||||||||||||
Full Title: Cognitive function after liver transplantation comparing Tacrolimus formulations | |||||||||||||
Medical condition: Immunosuppression post liver transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005043-13 | Sponsor Protocol Number: RG_14-187 | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Evaluating different rate control therapies in permanent atrial fibrillation: A prospective, randomised, open-label, blinded endpoint study comparing digoxin and beta-blockers as initial rate contr... | |||||||||||||
Medical condition: Atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002688-25 | Sponsor Protocol Number: CASM981CGB02 | Start Date*: 2005-01-07 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: A 4-week, randomized, multicenter, parallel-group, placebo-controlled study to investigate the effect of Elidel (pimecrolimus) cream 1% on the Quality of Life (QoL) of patients with moderate facial... | ||
Medical condition: Atopic Eczema (AE) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004427-19 | Sponsor Protocol Number: 807 41 002 | Start Date*: 2006-02-21 | |||||||||||
Sponsor Name:Ludwig-Maximilians-Universitaet Muenchen | |||||||||||||
Full Title: Health-related quality of life (QoL) and psychological well-being after withdrawal from hormone therapy (HT). A randomised double-blind placebo-controlled trial. | |||||||||||||
Medical condition: Menopause and female climacteric states | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002335-33 | Sponsor Protocol Number: KKS287 | Start Date*: 2022-05-18 | |||||||||||
Sponsor Name:Philipps University Marburg | |||||||||||||
Full Title: Inhaled ColiFin® in adult bronchiectasis patients with new asymptomatic Pseudomonas aeruginosa infection– an open-label, proof of concept - randomized controlled trial | |||||||||||||
Medical condition: bronchiectasis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001334-26 | Sponsor Protocol Number: ARC008 | Start Date*: 2018-01-17 |
Sponsor Name:Aimmune Therapeutics, Inc. | ||
Full Title: A MULTICENTER, OPEN-LABEL, LONG-TERM SAFETY STUDY OF AR101 CHARACTERIZED ORAL DESENSITIZATION IMMUNOTHERAPY IN SUBJECTS WHO PARTICIPATED IN A PRIOR AR101 STUDY | ||
Medical condition: Peanut Allergy | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) IE (Prematurely Ended) SE (Completed) ES (Completed) DE (Completed) FR (Prematurely Ended) NL (Prematurely Ended) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002922-51 | Sponsor Protocol Number: H6D-MC-LVGH | Start Date*: 2006-10-16 | |||||||||||
Sponsor Name:Lilly ICOS LLC | |||||||||||||
Full Title: Tadalafil 5 mg Once a Day Compared to Placebo in Improving Erectile Dysfunction and Sexual Quality of Life | |||||||||||||
Medical condition: Erectile Dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001707-31 | Sponsor Protocol Number: Protocolversion1.0 | Start Date*: 2015-07-10 |
Sponsor Name:Hull & East Yorkshire Hospitals NHS Trust | ||
Full Title: The SCaIPEL study: Survival and Quality of Life of Cancer Patients with Incidental Pulmonary Embolism Treated with LMWH | ||
Medical condition: Incidental Pulmonary Embolism in Cancer Patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2022-002241-18 | Sponsor Protocol Number: 983.974.742 | Start Date*: 2023-03-14 |
Sponsor Name:Helse Bergen HF | ||
Full Title: Diagnostic treatment-trial for autonomous cortisol secretion- a tool to select patients for adrenalectomy | ||
Medical condition: autonomous cortisol secretion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003630-33 | Sponsor Protocol Number: ERGO45359 | Start Date*: 2019-01-23 | |||||||||||
Sponsor Name:University of Southampton | |||||||||||||
Full Title: Spironolactone for Adult Female Acne: A pragmatic multicentre double-blind randomised superiority trial to investigate the clinical and cost-effectiveness of spironolactone for moderate or severe p... | |||||||||||||
Medical condition: Acne of sufficient severity to warrant treatment with oral antibiotics. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005262-35 | Sponsor Protocol Number: 16401 | Start Date*: 2013-07-08 | ||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||
Full Title: BENEFIT 11 a long-term, follow-up study (16401) of the BENEFIT (304747), BENEFIT Follow-up (305207) Studies and BENEFIT Extension (311129) Study to further evaluate the progress of patients with fi... | ||||||||||||||||||
Medical condition: Clinically isolated syndrome (CIS) and multiple sclerosis (MS) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) SE (Completed) PT (Completed) HU (Completed) CZ (Completed) NO (Completed) AT (Completed) FI (Completed) DK (Completed) GB (Completed) ES (Completed) IT (Completed) SI (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018209-32 | Sponsor Protocol Number: DHEA091209 | Start Date*: 2010-02-17 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: EFFECTS OF DHEA TREATMENT ON ANTHROPOMETRIC AND METABOLIC PARAMETERS, AND ON QUALITY OF LIFE (QOL) IN PATIENTS WITH ADDISON S DISEASE UNDER GLUCORTICOID-MINERALCORTICOID SUBSTITUTIVE TREATMENT | |||||||||||||
Medical condition: Addison s disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004526-72 | Sponsor Protocol Number: 1 | Start Date*: 2006-03-02 |
Sponsor Name:Addenbrooke's NHS Trust | ||
Full Title: A randomised controlled study of continuous subcutaneous insulin infusion (CSII) therapy compared to conventional bolus insulin treatment in preschool aged children with Type 1 diabetes. | ||
Medical condition: Type 1 Diabetes Mellitus | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-004991-16 | Sponsor Protocol Number: tba | Start Date*: 2022-09-28 |
Sponsor Name: | ||
Full Title: 177Lu-PSMA RADIOLIGAND THERAPY IN PATIENTS WITH LYMPH NODE METASTATIC HORMONE-SENSITIVE PROSTATE CANCER UNDERGOING ROBOT-ASSISTED LAPAROSCOPIC RADICAL PROSTATECTOMY AND EXTENDED PELVIC LYMPH NODE D... | ||
Medical condition: prostate cancer, eligible for radical prostatectomy and extended pelvic lymph node dissection, with 1-3 pelvic nodal metastases on preoperative PSMA PET | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000284-14 | Sponsor Protocol Number: | Start Date*: 2016-01-05 |
Sponsor Name:University of Calgary | ||
Full Title: Assessment of Metoprolol in the Prevention of Vasovagal Syncope in Aging Subjects | ||
Medical condition: Vasovagal Syncope | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000821-37 | Sponsor Protocol Number: O3NPIQ | Start Date*: 2019-12-10 | |||||||||||
Sponsor Name:Bernardino Clavo - Hospital Universitario de G. C. Dr. Negrín | |||||||||||||
Full Title: Effectiveness and cost-effectiveness of Ozone therapy in patients with pain secondary to chemotherapy-induced peripheral neuropathy. Randomized, triple-blind clinical trial. | |||||||||||||
Medical condition: Pain secondary to chemotherapy-induced peripheral neuropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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