- Trials with a EudraCT protocol (2,316)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,316 result(s) found.
Displaying page 17 of 116.
| EudraCT Number: 2012-005797-58 | Sponsor Protocol Number: 465 | Start Date*: 2013-04-19 | ||||||||||||||||
| Sponsor Name:Kvinnokliniken, Universitetessjukhuset i Linköping, landstinget i Östergötland | ||||||||||||||||||
| Full Title: Contraception after gastric bypass - part three How does gastric bypass affect the pharmacocinetics of oral desogestrel? | ||||||||||||||||||
| Medical condition: We want to investigate how the pharmacocinetics changes for Cerazette in 14 fertile obese women after, compared to before, bariatric surgery in forms of gastric by pass. Mesures of serum concetrati... | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: SE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-002751-38 | Sponsor Protocol Number: PREPREP | Start Date*: 2021-02-01 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Long-term effect of chlorhexidine gluconate 4% and Chlorhexidine alcohol 5 mg /ml on growth and recolonisation of bacteria on the skin | ||
| Medical condition: Cutaneous antibacterial efficacy in healthy volunteers. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000861-34 | Sponsor Protocol Number: 2021-000861-34 | Start Date*: 2022-07-01 |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Comparison of albumin and Ringer´s solution for optimization of the plasma volume and hemodynamics during surgery. | ||
| Medical condition: Patients in need of major laparoscopic surgery in the abdomen, lasting longer than 90 minutes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001873-25 | Sponsor Protocol Number: vers20130714 | Start Date*: 2013-08-29 |
| Sponsor Name:County Council of Östergötland | ||
| Full Title: Will intrathecal analgesia contribute to a faster recovery compared with epidural analgesia after open surgery for gynecological cancer. An open controlled randomized study. | ||
| Medical condition: Recovery after open abdominal surgery for gynecological cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000867-21 | Sponsor Protocol Number: NGAM-13 | Start Date*: 2021-08-16 |
| Sponsor Name:Octapharma Pharmazeutika Produktionsges.m.b.H. | ||
| Full Title: A Superiority Study To Compare The Effect of Panzyga Versus Placebo in Patients with Pediatric Acute-onset Neuropsychiatric Syndrome | ||
| Medical condition: Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS). PANS is a research diagnosis given to patients who have an abrupt, dramatic onset of neuropsychiatric symptoms including obsessions/compulsio... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-005441-32 | Sponsor Protocol Number: DIAGNODE-B | Start Date*: 2021-12-28 | |||||||||||
| Sponsor Name:Linköping University | |||||||||||||
| Full Title: DIAGNODE-B, A Phase I/II Open Label Pilot Study to evaluate the safety and feasibility of an additional intralymphatic booster administration of GAD-alum (Diamyd®) in individuals with Type 1 diabetes | |||||||||||||
| Medical condition: Type 1 diabetes mellitus | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002895-42 | Sponsor Protocol Number: GITS2013_4.0 | Start Date*: 2013-10-10 | ||||||||||||||||
| Sponsor Name:Region Västerbotten | ||||||||||||||||||
| Full Title: Glaucoma Intensity Treatment Study – Intensive non-invasive glaucoma treatment vs conventional stepwise treatment – a prospective, randomized phase IV study of disease progression in glaucoma (GITS... | ||||||||||||||||||
| Medical condition: Glaucoma, open-angle and PEX glaucoma. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-000050-22 | Sponsor Protocol Number: SEGCG18-01 | Start Date*: 2018-04-24 | |||||||||||
| Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
| Full Title: Irinotecan-based triplet (FOLFOXIRI) as perioperative treatment in resectable gastric and gastroesophageal junction adenocarcinoma. | |||||||||||||
| Medical condition: Resectabel gastric and gastroesophageal junction adenocarcinoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004187-35 | Sponsor Protocol Number: FACE-01 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Falun Hospital | |||||||||||||
| Full Title: The FACE (Facial nerve palsy And Cortisone Evaluation) study in children: a randomised double-blind, placebo-controlled, multicenter trial. | |||||||||||||
| Medical condition: Facial Nerve Palsy (Bells Palsy) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000823-11 | Sponsor Protocol Number: TIMO | Start Date*: 2023-03-09 | ||||||||||||||||
| Sponsor Name:Sahlgrenska University Hospital Gothenburg | ||||||||||||||||||
| Full Title: Ticagrelor monotherapy after coronary stenting in patients with acute myocardial infarction. A prospective single-centre, single-arm phase II study | ||||||||||||||||||
| Medical condition: Antiplatelet therapy in patients who undergo coronary artery stenting due to coronary artery disease (CAD) or acute coronary syndrome (ACS). The present study will examine whether ticagrelor, as mo... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-002367-21 | Sponsor Protocol Number: DiaSpax | Start Date*: 2021-11-01 | |||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
| Full Title: Fettvävsheterogenitet och dess koppling till typ 2 diabetes : En randomiserad öppen behandlingsstudie som jämför Empagliflozin, Pioglitazon och Semaglutide | |||||||||||||
| Medical condition: Diabetes typ 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004704-35 | Sponsor Protocol Number: BTX1-myalgia_pain | Start Date*: 2020-05-18 |
| Sponsor Name:Region Örebro | ||
| Full Title: Masseter myofascial pain relief following an intra-muscular injection with botulinum toxin type A. A randomized double-blind controlled multicenter pilot study. | ||
| Medical condition: Myalgia of jaw muscle | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-001249-11 | Sponsor Protocol Number: Parachutes | Start Date*: 2021-07-14 | |||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
| Full Title: PARACHUTES: Pedophilia At Risk – Acute Treatment – E-therapy vs SSRI | |||||||||||||
| Medical condition: Pedophilic Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002356-39 | Sponsor Protocol Number: D/P2/22/8 | Start Date*: 2022-12-14 | |||||||||||
| Sponsor Name:Diamyd Medical AB | |||||||||||||
| Full Title: DiaPrecise, A Phase II Open Label Study to evaluate the safety and feasibility of intralymphatic administration of Diamyd® in individuals at risk for Type 1 diabetes carrying the HLA DR3-DQ2 haplotype | |||||||||||||
| Medical condition: Stage 1 or stage 2 pre-type1 diabetes (seropositive for two or more T1D–associated autoantibodies) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004244-28 | Sponsor Protocol Number: BAN2401-G000-303 | Start Date*: 2023-04-17 | |||||||||||
| Sponsor Name:Eisai Ltd. | |||||||||||||
| Full Title: AHEAD 3-45 Study: A Placebo-Controlled, Double-Blind, Parallel Treatment Arm, 216 Week Study with an Extension Phase to Evaluate Efficacy and Safety of Treatment With BAN2401 in Subjects With Prec... | |||||||||||||
| Medical condition: Preclinical Alzheimer's Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000652-11 | Sponsor Protocol Number: SPAGOPIX-02 | Start Date*: 2022-08-17 | |||||||||||
| Sponsor Name:Spago Nanomedical AB | |||||||||||||
| Full Title: A Phase IIa, single centre, open label, proof of concept study concerning efficacy of the novel intravenous contrast agent SN132D in patients with suspected endometriosis. | |||||||||||||
| Medical condition: Suspected endometriosis | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000462-41 | Sponsor Protocol Number: MTXRA | Start Date*: 2021-02-09 |
| Sponsor Name:Västerbotten county | ||
| Full Title: Efficacy, tolerability and preferences of peroral or subcutaneous methotrexate in patients with early rheumatoid arthritis – a randomized register based multicenter study | ||
| Medical condition: Rheumatoid arthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001489-41 | Sponsor Protocol Number: P00003466 | Start Date*: 2018-07-02 | |||||||||||
| Sponsor Name:Karolinska Universitetssjukhuset | |||||||||||||
| Full Title: Radiation- and alkylator-free hematopoietic cell transplantation for bone marrow failure due to dyskeratosis congenita / telomere disease | |||||||||||||
| Medical condition: Dyskeratosis congenita / telomere disease | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004960-20 | Sponsor Protocol Number: 58246 | Start Date*: 2017-03-29 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Local zoledronate for improved fixation of uncemented hip prostheses. | ||
| Medical condition: Prosthetic migration in uncemented total hip replacement | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003300-12 | Sponsor Protocol Number: LOKON003 | Start Date*: 2019-12-20 | |||||||||||
| Sponsor Name:Lokon Pharma AB | |||||||||||||
| Full Title: A Phase I/II Trial Investigating LOAd703 in Combination with Atezolizumab in Malignant Melanoma | |||||||||||||
| Medical condition: Malignant melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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