- Trials with a EudraCT protocol (380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
380 result(s) found for: General Health Questionnaire.
Displaying page 1 of 19.
EudraCT Number: 2019-002848-24 | Sponsor Protocol Number: IFT2019 | Start Date*: 2020-03-06 |
Sponsor Name:GIGA-Consciousness Thematic Unit, Anesthesia and Intensive Care Laboratory, Liege University | ||
Full Title: Brain functional signature of connected consciousness under general anesthesia using the isolated forearm technique | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000967-42 | Sponsor Protocol Number: IIV-276 | Start Date*: 2014-05-20 |
Sponsor Name:National Institute for Public Health and the Environment (RIVM) | ||
Full Title: Strengthening memory immunity in the aged population by vaccinating re-elderly | ||
Medical condition: The vaccine administered in this study is used to prevent meningococcal disease caused by the bacteria Neisseria meningitidis group A,C,W,Y (Nimenrix) and Herpes Zoster disease caused by the Vari... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000991-13 | Sponsor Protocol Number: STH19610 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: The MAGIC trial (Melatonin for Anxiety prior to General anaesthesia In Children): A Multicentre, Parallel Randomised Controlled Trial of Melatonin Versus Midazolam in the Premedication of Anxious C... | ||||||||||||||||||||||||||||
Medical condition: Anxiety pre-general anaesthesia | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003658-26 | Sponsor Protocol Number: unknown | Start Date*: 2013-11-13 |
Sponsor Name:VU University Medical Center | ||
Full Title: Treat-to-target strategy for early RA patients in usual clinical practice: The COBRA Cohort Study | ||
Medical condition: Early Active Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004555-79 | Sponsor Protocol Number: 16-115 | Start Date*: 2017-08-08 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: Impact of preoperative midazolam on outcome of elderly patients: a multicenter randomised controlled trial | ||
Medical condition: Under investigation are elderly patients (≥65 years of age) undergoing each kind of surgery with planned general or combined regional and general anaesthesia. Primary, we will investigate the posto... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001552-37 | Sponsor Protocol Number: RG07-066(FormerlyHTA02/06/02) | Start Date*: 2008-07-25 |
Sponsor Name:University of Birmingham | ||
Full Title: Effectiveness and Cost-effectiveness of Levonorgestrel containing Intrauterine system in Primary care against Standard Treatment for menorrhagia | ||
Medical condition: Menorrhagia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002135-30 | Sponsor Protocol Number: NCT04379973 | Start Date*: 2021-04-28 |
Sponsor Name:Antwerp University Hospital (UZA) | ||
Full Title: Live birth after additional tubal flushing with oil-based contrast versus no additional flushing: a randomised, multicentre, parallel group pragmatic trial in infertile women with at least one pate... | ||
Medical condition: Infertility defined as lack of conception despite 12 months of unprotected intercourse, or three cycles of donor insemination without pregnancy or three ovulatory ovulation induction cycles without... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004362-26 | Sponsor Protocol Number: I3Y-MC-JPCF | Start Date*: 2017-08-14 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Study of Abemaciclib Combined with Standard Adjuvant Endocrine Therapy versus Standard Adjuvant Endocrine Therapy Alone in Patients with High-Risk, Node-Positive, ... | |||||||||||||
Medical condition: Node Positive, Early Stage, Hormone Receptor Positive, Human Epidermal Receptor 2 Negative, Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) HU (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) DK (Trial now transitioned) FI (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) CZ (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002787-32 | Sponsor Protocol Number: RG_19-172 | Start Date*: 2020-11-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Antidepressant for the prevention of DEPression following first episode Psychosis trial | ||
Medical condition: Patients with First Episode Psychosis. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003341-10 | Sponsor Protocol Number: NL47979.091.14 | Start Date*: 2018-01-16 |
Sponsor Name:Rijnstate | ||
Full Title: Registry of the treatment of primay insufficiency of the great saphenous vein with a diameter >/= 12 mm, anterolateral branches, or great saphenous vein insufficiency below the knee with mechano-... | ||
Medical condition: varicose veins of the infragenual great saphenous vein, large supragenual great saphenous vein (>= 12 mm) and antero-lateral branch varicose veins | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-024189-23 | Sponsor Protocol Number: DR-CR-NEU01S01 | Start Date*: 2011-08-31 | |||||||||||
Sponsor Name:Weleda AG | |||||||||||||
Full Title: Efficacy and safety of Neurodoron in patients with nervous exhaustion - a randomized, double-blind, placebo-controlled clinical trial | |||||||||||||
Medical condition: nervous exhaustion (neurasthenia) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003052-70 | Sponsor Protocol Number: APAC2016 | Start Date*: 2016-11-10 | |||||||||||
Sponsor Name:Academic Medical Center of Amsterdam | |||||||||||||
Full Title: Initial non-operative treatment strategy versus appendectomy treatment strategy for simple appendicitis in children aged 7-17 years old. APAC study | |||||||||||||
Medical condition: Acute uncomplicated (simple) appendicitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002156-27 | Sponsor Protocol Number: 1356/2015 | Start Date*: Information not available in EudraCT |
Sponsor Name:Medical University of Vienna | ||
Full Title: Prospective controlled study of reduced-dose Rituximab in rheumatoid arthritis patients in low disease activity and remission – the REDOREM study | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-002802-21 | Sponsor Protocol Number: PRIMERA001 | Start Date*: 2020-12-18 | ||||||||||||||||
Sponsor Name:Erasmus Medical Center | ||||||||||||||||||
Full Title: PeRsonalIzed MEdicine in Rheumatoid Arthritis (PRIMERA trial): a multicenter, single-blinded, randomized controlled trial comparing usual care with a tailor-made approach | ||||||||||||||||||
Medical condition: Rheumatoid arthritis according to 2010 criteria | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004737-37 | Sponsor Protocol Number: CORTERAS | Start Date*: 2021-11-16 | |||||||||||
Sponsor Name:Ziekenhuis Oost-Limburg | |||||||||||||
Full Title: The effect of corticosteroids on early recovery after major surgery in elderly patients_ CORTERAS STUDY | |||||||||||||
Medical condition: major surgery • off-pump coronary bypass surgery • on-pump coronary bypass surgery • Aortic Valve Replacement Mini Access Surgery • laparoscopic hemicolectomies • thoracoscopic lung resections • fe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003929-30 | Sponsor Protocol Number: 1 | Start Date*: 2022-10-14 |
Sponsor Name:Ligalli BV | ||
Full Title: INFLUENCE OF OXYBUTYNIN - MEDRING LIGALLI ON OVERACTIVE BLADDER SYMPTOMS IN WOMEN | ||
Medical condition: urinary urge incontinence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001289-14 | Sponsor Protocol Number: MIT-Do001-C301 | Start Date*: 2020-02-05 | |||||||||||
Sponsor Name:Estetra SRL | |||||||||||||
Full Title: A Randomized Double-blind Placebo Controlled Phase 3 Trial to evaluate the Efficacy and Safety of Estetrol for the Treatment of Moderate to Severe Vasomotor Symptoms in Postmenopausal Women (E4Comf... | |||||||||||||
Medical condition: Moderate to Severe Vasomotor Symptoms (VMS) in Postmenopausal Women | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Completed) GB (GB - no longer in EU/EEA) SK (Completed) HU (Completed) LT (Completed) CZ (Completed) ES (Completed) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004335-23 | Sponsor Protocol Number: CBD-FEP | Start Date*: 2013-12-30 | ||||||||||||||||
Sponsor Name:Central Institute of Mental Health | ||||||||||||||||||
Full Title: A four-week, multicentre, double-blinded, randomised, active- and placebo-controlled, parallel-group trial investigating efficacy and safety of cannabidiol in acute, early-stage schizophrenic patie... | ||||||||||||||||||
Medical condition: Acute early-stage psychosis | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Temporarily Halted) DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004359-35 | Sponsor Protocol Number: ICEA2020.1 | Start Date*: 2020-10-23 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Induction of Cure in Early Arthritis | |||||||||||||
Medical condition: early unclassified arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001068-27 | Sponsor Protocol Number: 2020-001068-27 | Start Date*: 2020-12-01 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Pamidronate for pain in adult chronic nonbacterial osteitis (PAM-CNO): a randomized, double-blind, placebo-controlled trial | ||
Medical condition: Chronic nonbacterial osteitis (CNO) in adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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