- Trials with a EudraCT protocol (1,226)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,226 result(s) found for: Patient-reported outcomes.
Displaying page 1 of 62.
EudraCT Number: 2019-004007-12 | Sponsor Protocol Number: 066VER | Start Date*: 2020-06-02 |
Sponsor Name:University of Sussex | ||
Full Title: Brain connectivity and patient reported outcomes in people with HIV (PWH) with symptoms of insomnia switching integrase inhibitor-based ART; a randomised controlled study | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004354-15 | Sponsor Protocol Number: DANPAPP | Start Date*: 2017-12-13 | ||||||||||||||||
Sponsor Name: Rigshospitalet | ||||||||||||||||||
Full Title: Prevalence, pattern and disease course of arthritis and enthesitis in patients with psoriasis, and the effect of apremilast in subclinical US-defined psoriatic arthritis - A population-based study ... | ||||||||||||||||||
Medical condition: Psoriasis and psoriatic arthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001077-87 | Sponsor Protocol Number: IJB-RT-HNC-001 | Start Date*: 2019-08-08 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Patient reported outcomes in term of swallowing and quality of life after prophylactic versus reactive percutaneous endoscopic gastrostomy tube placement in advanced head and neck cancer patients t... | |||||||||||||
Medical condition: advanced head and neck cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003808-39 | Sponsor Protocol Number: MK-3475-866 | Start Date*: 2019-07-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: A Phase 3, Randomized Double Blind Study to Evaluate Peri-operative Pembrolizumab (MK-3475) + Neoadjuvant Chemotherapy versus Perioperative Placebo + Neoadjuvant Chemotherapy in Cisplatin-Eligible ... | |||||||||||||
Medical condition: Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) IE (Trial now transitioned) DE (Trial now transitioned) GB (GB - no longer in EU/EEA) DK (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000505-72 | Sponsor Protocol Number: 2019-000505-72 | Start Date*: 2019-05-13 |
Sponsor Name:Transparency in Healthcare | ||
Full Title: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Medical condition: Pragmatic trial baricitinib versus First biological in “Tight Control” Patients suffering from Rheumatoid Arthritis (PERFECT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024017-31 | Sponsor Protocol Number: CFTY720DIT02 | Start Date*: 2011-03-15 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 6-month, Randomized, Active Comparator, Open-label, Multi-Center Study to Evaluate Patient OutComes, Safety and Tolerability of Fingolimod (FTY720) 0.5 mg/day in Patients with Relapsing Remitting... | |||||||||||||
Medical condition: Relapsing Remitting Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003844-11 | Sponsor Protocol Number: ML29242 | Start Date*: 2015-04-27 |
Sponsor Name:Department of Oncology, Linköping University Hospital, Linköping, Sweden | ||
Full Title: Continous treatment with bevacizumab in elderly patients with mCRC: an open label, single arm, prospective phase IV trial to evaluate outcome and safety of continuous bevacizumab treatment in combi... | ||
Medical condition: Metastatic colorectal cancer | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-005686-12 | Sponsor Protocol Number: RD.03.SPR.29107 | Start Date*: 2013-05-23 | |||||||||||
Sponsor Name:Galderma R&D | |||||||||||||
Full Title: Patient-reported outcomes of Brimonidine Tartrate 0.5% gel for treatment of severe facial erythema of rosacea | |||||||||||||
Medical condition: Erythema of rosacea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004078-40 | Sponsor Protocol Number: CQR14002 | Start Date*: 2015-01-28 | |||||||||||
Sponsor Name:CeQur Corp. | |||||||||||||
Full Title: A Prospective, Single Center, Observational Study to Assess the Performance, Safety, and Patient Reported Outcomes of Insulin Delivery with PaQ® in Patients with Type 2 Diabetes Mellitus | |||||||||||||
Medical condition: Type 2 diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004179-38 | Sponsor Protocol Number: PULMORA | Start Date*: 2020-01-10 | |||||||||||
Sponsor Name:Västra Götalandsregionen | |||||||||||||
Full Title: Effects of tofacitinib vs methotrexate on clinical and molecular disease activity markers in joints and lungs in early rheumatoid arthritis | |||||||||||||
Medical condition: Patients with early active rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003382-10 | Sponsor Protocol Number: PazoQol | Start Date*: 2018-02-28 | |||||||||||||||||||||
Sponsor Name:GWT-TUD GmbH | |||||||||||||||||||||||
Full Title: Quality of life in patients with non-adipocyte soft tissue sarcoma under palliative chemotherapy or pazopanib – a randomized, controlled trial- PazoQoL | |||||||||||||||||||||||
Medical condition: Soft tissue sarcoma (STS) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002978-52 | Sponsor Protocol Number: CNTO1959HDS2002 | Start Date*: 2019-07-16 |
Sponsor Name:Universitair Medisch Centrum Groningen | ||
Full Title: Guselkumab for hidradenitis suppurativa, a mode of action study. | ||
Medical condition: Hidradenitis suppurativa | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023512-13 | Sponsor Protocol Number: CAIN457A2302 | Start Date*: 2011-05-24 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multi-center study of subcutaneous secukinumab to demonstrate efficacy after twelve weeks of treatment, and to assess the safety, tolerability and lo... | |||||||||||||
Medical condition: Moderate to severe chronic plaque-type psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) IS (Completed) EE (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004795-19 | Sponsor Protocol Number: 120824001 | Start Date*: 2013-03-12 | |||||||||||
Sponsor Name:Folktandvården Västra Götaland | |||||||||||||
Full Title: Utilisation of botulinum toxin type A on masticatory muscel hyperactivity in CP - a randomized, controlled study. | |||||||||||||
Medical condition: Masticatory muscle hyperactivity/bruxism in patients with Cerebral Palsy. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002134-14 | Sponsor Protocol Number: 1.0 | Start Date*: 2022-09-02 |
Sponsor Name:Catharina Hospital Eindhoven | ||
Full Title: Intraperitoneal irinotecan with concomitant FOLFOX and bevacizumab for patients with unresectable colorectal peritoneal metastases – a phase II study | ||
Medical condition: Patients with peritoneal carcinomatosis of colorectal origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005228-27 | Sponsor Protocol Number: INTERIM17 | Start Date*: 2017-10-05 |
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||
Full Title: INTERIM: a randomised phase II feasibility study of INTERmittent versus continuous dosing of oral targeted combination therapy In patients with BRAFV600 mutant stage 3 unresectable or metastatic Me... | ||
Medical condition: BRAFV600 mutant stage 3 unresectable or metastatic melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2018-004476-35 | Sponsor Protocol Number: CCFZ533B2201 | Start Date*: 2019-08-19 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 48-week, 6-arm, randomized, double-blind, placebo-controlled multicenter trial to assess the safety and efficacy of multiple CFZ533 doses administered subcutaneously in two distinct populations o... | |||||||||||||
Medical condition: Sjögren syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) FR (Completed) DE (Completed) SE (Completed) AT (Completed) SI (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000996-17 | Sponsor Protocol Number: 201200099617 | Start Date*: 2012-06-18 |
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||
Full Title: Phase II study of biweekly cabazitaxel in patients affected by castration resistant prostate cancer previously treated with docetaxel: evaluation of safety and quality of life. | ||
Medical condition: Subjects affected by metastatic castration refractory prostate cancer progressed or intolerant to a previous docetaxel-based chemotherapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002202-37 | Sponsor Protocol Number: 2015-115 | Start Date*: 2016-01-06 |
Sponsor Name:radboudumc | ||
Full Title: Pilot study: Is concomitant administration of lidocaine during oxaliplatin infusion able to prevent pain as a result of oxaliplatin induced acute neuropathy? | ||
Medical condition: Acute oxaliplatin induced neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001656-35 | Sponsor Protocol Number: 109MS408 | Start Date*: 2014-04-07 | ||||||||||||||||
Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
Full Title: A Multicenter, Open-Label Study Evaluating the Effectiveness of Oral Tecfidera™ (Dimethyl Fumarate) on MS Disease Activity and Patient-Reported Outcomes in Subjects with Relapsing-Remitting Multipl... | ||||||||||||||||||
Medical condition: Relapsing-Remitting Multiple Sclerosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) HU (Completed) BE (Completed) PT (Completed) IT (Completed) CZ (Completed) SK (Completed) ES (Completed) SI (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
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