- Trials with a EudraCT protocol (333)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
333 result(s) found for: Difference in differences.
Displaying page 1 of 17.
| EudraCT Number: 2019-001843-37 | Sponsor Protocol Number: 52649 | Start Date*: 2019-08-06 | ||||||||||||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||||||||||||
| Full Title: Imaging of tumour microenvironment in patients with oropharyngeal head and neck squamous cell carcinoma using RGD PET/CT imaging. | ||||||||||||||||||||||||||||
| Medical condition: The aim of this study is to assess differences in tumour microenvironment between HPV positive and HPV negative oropharyngeal head and neck squamous cell carcinoma using [68Ga]Ga-RGD2 PET/CT and p... | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-002640-82 | Sponsor Protocol Number: EANITIATE1 | Start Date*: 2018-11-20 | |||||||||||
| Sponsor Name:Nordsjællands Hospital | |||||||||||||
| Full Title: A randomized, controlled, multicentre trial regarding the safety and feasibility of treatment with empagliflozin compared with NPH insulin treatment in patients with newly onset diabetes following ... | |||||||||||||
| Medical condition: Diabetes Mellitus that is induced by the use of glucocorticoids | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-000502-30 | Sponsor Protocol Number: DKFZ-2019-001 | Start Date*: 2020-03-26 | |||||||||||||||||||||
| Sponsor Name:German Cancer Research Center (DKFZ) | |||||||||||||||||||||||
| Full Title: Personalized Vitamin D Supplementation for Reducing or Preventing Fatigue and Enhancing Quality of Life of Patients with Colorectal Tumor: Randomized Intervention Trial | |||||||||||||||||||||||
| Medical condition: Fatigue in patients with colorectal cancer (ICD codes C18-C20 and C21.8) within 12 months after a colorectal cancer therapy (surgery, chemotherapy and/ or radiation) and not optimal vitamin D status | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2014-005156-26 | Sponsor Protocol Number: PRIN-SUGAR-2014 | Start Date*: 2015-05-27 |
| Sponsor Name:Dr. Enrique Alday | ||
| Full Title: Effects of neuromuscular block reversal with sugammadex vs neostigmine on postoperative respiratory outcomes after major abdominal surgery. A randomized controlled trial. | ||
| Medical condition: Patients of both sexes proposed for major abdominal surgery under general anesthesia plus epidural | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001025-20 | Sponsor Protocol Number: ROPIOBES_HULP_2018 | Start Date*: 2018-05-25 |
| Sponsor Name:Servicio de Anestesiología y Reanimación del Hospital Universitario La Paz | ||
| Full Title: COMPARISON OF POSTOPERATIVE ANALGESIA OF INTRAPERITONEAL NEBULIZED ROPIVACAIN BEFORE AND AFTER LAPAROSCOPIC GASTRIC BY-PASS IN OBESITY SURGERY | ||
| Medical condition: Post-surgical pain after gastric bypass surgery in obese patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002678-10 | Sponsor Protocol Number: GF22002 | Start Date*: 2023-03-07 |
| Sponsor Name:Ginefiv | ||
| Full Title: Protocol with progestin-primed ovarian stimulation (PPOS) starting on day 5 versus protocol with progestin-primed ovarian stimulation (PPOS) in a conventional regimen from the start of the ovaria... | ||
| Medical condition: Number of MII oocytes obtained in both groups | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003451-42 | Sponsor Protocol Number: 19642021 | Start Date*: 2021-12-23 | |||||||||||
| Sponsor Name:Dept. of Growth and Reproduction | |||||||||||||
| Full Title: FITMI - First In Treating Male Infertility | |||||||||||||
| Medical condition: Male infertility | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005215-16 | Sponsor Protocol Number: CHUB-MentalRecup001 | Start Date*: 2015-02-13 | |||||||||||
| Sponsor Name:CHU Brugmann | |||||||||||||
| Full Title: A psychomotor recuperation study after deep sedation for colonoscopy between target controlled and manual titration of propofol. | |||||||||||||
| Medical condition: Ambulatory colonoscopy with sedation by target controlled infusion or manual titration of propofol. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000272-26 | Sponsor Protocol Number: HYKP1021 | Start Date*: 2014-09-04 |
| Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | ||
| Full Title: A Multicentre Phase III Double-masked Randomised Controlled Non-Inferiority Trial comparing the clinical and cost effectiveness of intravitreal therapy with ranibizumab (Lucentis) vs aflibercept (E... | ||
| Medical condition: Macular Oedema due to Central Retinal Vein Occlusion (CRVO). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-005271-12 | Sponsor Protocol Number: MetForMe | Start Date*: 2021-05-03 |
| Sponsor Name:Erasmus MC, Department of Dermatology | ||
| Full Title: Rediscovery of metformin for the chronic disabling auto-inflammatory disease hidradenitis suppurativa | ||
| Medical condition: Hidradenitis suppurativa | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001342-18 | Sponsor Protocol Number: IB-0319-001 | Start Date*: 2019-08-19 |
| Sponsor Name:Instituto Bernabeu | ||
| Full Title: CONVENTIONAL STIMULATION IN FOLICULAR PHASE VS. STIMULATION IN LUTEA PHASE IN PATIENTS WITH SUBOPTIMA RESPONSE. RANDOMIZED CLINICAL TRIAL. SUBLUTEAL STUDY | ||
| Medical condition: Suboptimal response of ovarian stimulation | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-005019-16 | Sponsor Protocol Number: ROCKSAN | Start Date*: 2009-03-19 |
| Sponsor Name:AMC- academisch psychiatrisch centrum | ||
| Full Title: Randomized Olanzapine Clozapine Key study on Schizophrenia and Addiction in the Netherlands (ROCKSAN) | ||
| Medical condition: A multi-centre prospective, randomized, double blind designed study examining the effectiveness and costs of clozapine compared to olanzapine in patients with schizophrenia or related psychotic dis... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004433-93 | Sponsor Protocol Number: RIOTCSTUDY22017 | Start Date*: 2018-05-01 | ||||||||||||||||
| Sponsor Name:Nicholas Stephen Macklon, Professor, MD, PhD | ||||||||||||||||||
| Full Title: RIOT C: REDUCING THE IMPACT OF OVARIAN STIMULATION. NOVEL APPROACHES TO LUTEAL SUPPORT IN IVF. STUDY 2. | ||||||||||||||||||
| Medical condition: Ovarian stimulation in oocyte donation | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-000099-27 | Sponsor Protocol Number: HEAT01 | Start Date*: 2017-04-26 | |||||||||||
| Sponsor Name:The Department of Urology | |||||||||||||
| Full Title: Toxicity of first-line abiraterone versus enzalutamide in men with metastatic castration-resistant prostate cancer: A randomized clinical trial | |||||||||||||
| Medical condition: Metastisc castration resistant prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000684-16 | Sponsor Protocol Number: reboundpainplexus | Start Date*: 2016-05-25 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Brachial plexus block and rebound pain after radius fixation with a polar plate. | ||
| Medical condition: Pain after radius fracture fixation by a volar plate. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001717-17 | Sponsor Protocol Number: P1901GF | Start Date*: 2019-10-23 | |||||||||||
| Sponsor Name:Pohl-Boskamp GmbH & Co. KG | |||||||||||||
| Full Title: A multi-centre, randomised, placebo-controlled, double-blind parallel-group trial to assess the efficacy and safety of SIA capsules in subjects with acute rhinosinusitis. | |||||||||||||
| Medical condition: acute rhinosinusitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-000999-41 | Sponsor Protocol Number: Evelien-01 | Start Date*: 2012-09-28 | |||||||||||
| Sponsor Name: | |||||||||||||
| Full Title: Effects of anatomical localization of the fentanyl patch on the pharmacokinetics and pharmacodynamics of fentanyl: a randomised cross-over trial | |||||||||||||
| Medical condition: cancer patients using a stable dose of a fentanyl patch as treatment for their continuous pain | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-002014-52 | Sponsor Protocol Number: FOOTSTEP | Start Date*: 2019-01-23 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: DUAL HOMING MECHANISMS OF EOSINOPHILS TO THE SPUTUM; ONLY ONE OF WHICH IS SENSITIVE FOR MEPOLIZUMAB | ||
| Medical condition: severe eosinophilic asthma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-021410-34 | Sponsor Protocol Number: EOC-2-Opht-2010 | Start Date*: 2010-08-12 | ||||||||||||||||
| Sponsor Name:Medical Centre Haaglanden | ||||||||||||||||||
| Full Title: A double blind randomized study on the efficacy of cyclopentolate 1% and cyclopentolate 1% with tropicamide 1% in children | ||||||||||||||||||
| Medical condition: Depth of cycloplegia; changes of astigmatism; recuperation from cycloplegia and mydriasis | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-003647-28 | Sponsor Protocol Number: NA | Start Date*: 2020-12-09 |
| Sponsor Name: | ||
| Full Title: Differences in antihypertensive drug levels in patients with hypertension: old vs young 2 | ||
| Medical condition: Hypertension Cardiovascular disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
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