- Trials with a EudraCT protocol (70)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (17)
70 result(s) found for: Antiemetic.
Displaying page 1 of 4.
EudraCT Number: 2015-000658-39 | Sponsor Protocol Number: AkupresSNP | Start Date*: 2016-07-11 |
Sponsor Name:Region Jönköpings län | ||
Full Title: Randomized multicenter study of Acupressure combined with personalized antiemetics based on genetic variations (SNPs) in women undergoing neoadjuvant or adjuvant chemotherapy EC / FEC against breas... | ||
Medical condition: Nausea in conjuction with neoadjuvant or adjuvant chemotherapy (FEC/EC) for patients with breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022872-30 | Sponsor Protocol Number: PALO-10-20 | Start Date*: 2011-08-04 | ||||||||||||||||
Sponsor Name:Helsinn Healthcare SA | ||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, parallel group study to evaluate the efficacy and safety of two different doses of palonosetron compared to ondansetron in the prevention of CINV in pediatr... | ||||||||||||||||||
Medical condition: Study to evaluate the efficacy and safety of two different doses of palonosetron compared to ondansetron in the prevention of CINV in pediatric patients undergoing single and repeated cycles of MEC... | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) HU (Completed) AT (Completed) BG (Completed) EE (Completed) DE (Completed) FR (Ongoing) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004031-37 | Sponsor Protocol Number: 17.14 | Start Date*: 2017-12-07 |
Sponsor Name:Department of oncology, Odense University Hospital | ||
Full Title: A multicentre, single-arm, phase II study to investigate the safety and antiemetic efficacy of Akynzeo® (a fixed dose combination of palonosetron and netupitant) plus dexamethasone in patients rece... | ||
Medical condition: Eligible patients will have a diagnosis of cervical cancer, and be scheduled to receive fractionated radiotherapy and concomitant weekly cisplatin at a dose of ≥ 40 mg/m2 for at least five weeks. P... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003316-20 | Sponsor Protocol Number: GIM15-NEPA | Start Date*: 2016-01-28 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||||||||||||||||||||||
Full Title: One day antiemetic prophylaxis of NEPA (netupitant plus palonosetron) and dexamethasone to prevent chemotherapy-induced nausea and vomiting (CINV) in breast cancer patients receiving a combination ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chemotherapy-Induced Nausea and Vomiting (CINV) in breast cancer patients receiving a combination chemotherapy of doxorubicin or epirubicin with cyclophosphamide (AC-based regimen) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005704-29 | Sponsor Protocol Number: LUNG-NEPA | Start Date*: 2016-06-08 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:CONSORZIO ONCOTECH | ||||||||||||||||||||||||||||||||||||||
Full Title: A standard regimen of dexamethasone in comparison to two dex-sparing regimens in addition to NEPA in preventing CINV in na¿ve NSCLC patients to be treated with cisplatin based chemotherapy: a three... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Chemotherapy-Induced Nausea and Vomiting (CINV) in non-small cell lung cancer (NSCLC) patients receiving a cisplatin-based chemotherapy | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001651-31 | Sponsor Protocol Number: 1.0 | Start Date*: 2017-11-30 |
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: EMPOWER: EMesis in Pregnancy - Ondansetron With mEtoclopRamide. | ||
Medical condition: Nausea and Vomiting in pregnancy Hyperemesis gravidarum | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011122-33 | Sponsor Protocol Number: EC08/00281 | Start Date*: 2009-07-09 |
Sponsor Name:FUNDACION PARA LA INVESTIGACION BIOMEDICA HOSPITAL 12 DE OCTUBRE | ||
Full Title: LA ANALGESIA DEL PARACETAMOL,¿DISMINUYE CUANDO SE ADMINISTRAN ANTIEMÉTICOS ANTISEROTONINÉRGICOS | ||
Medical condition: ANALGESIA POSTOPERATORIA AGUDA EN PROTESIS TOTAL DE RODILLA | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005700-15 | Sponsor Protocol Number: marha1983 | Start Date*: 2013-01-07 |
Sponsor Name:Lennart Svensson Linköping University Medical Faculty | ||
Full Title: Can 5-HT3 receptor antagonists be used to limit vomiting in rota- and norovirus infections? | ||
Medical condition: Virus caused vomiting and effect of the antiemetic drug Ondansetron | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001557-46 | Sponsor Protocol Number: 01 | Start Date*: 2012-06-27 |
Sponsor Name:Sydvestjysk Sygehus, Esbjerg [...] | ||
Full Title: Perioperativ installation of ropivacain in mastectomy – with or without axillary lymph node dissection after sentinel node diagnostics or known lymph node metastasis – A double-blind, randomized cl... | ||
Medical condition: Unilateral mastectomy with or without axillary lymph node dissection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-000781-37 | Sponsor Protocol Number: NKV102549 | Start Date*: 2006-07-24 |
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Active Controlled, Parallel Group Study of the Safety and Efficacy of the Intravenous and Oral Formulations of the Neurokinin-1 Receptor Antagon... | ||
Medical condition: Chemotherapy induced nausea and vomiting (CINV) due to Moderately Emetogenic Chemotherapy (MEC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) BE (Completed) IE (Completed) SK (Completed) ES (Completed) AT (Completed) EE (Completed) CZ (Completed) LT (Completed) HU (Completed) DK (Completed) LV (Completed) GR (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014717-27 | Sponsor Protocol Number: 2009/4:7 | Start Date*: 2009-12-22 |
Sponsor Name:Karolinska Institutet/Södersjukhuset | ||
Full Title: Betametasone as postoperative pain treatment for knee arthroscopies at a day surgical center | ||
Medical condition: Unspecified knee pain investigated by an arthroscopy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-002033-21 | Sponsor Protocol Number: NKV102551 | Start Date*: 2006-09-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Phase III Multicenter, Randomized, Double-Blind, Active-Controlled, Parallel Group Study of the Efficacy and Safety of the Intravenous and Oral Formulations of the Neurokinin-1 Receptor Antagonis... | |||||||||||||
Medical condition: Chemotherapy induced nausea and vomiting (CINV) due to Highly Emetogenic Chemotherapy (HEC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) IE (Completed) GR (Completed) BE (Completed) CZ (Completed) SK (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000732-22 | Sponsor Protocol Number: OSTAP | Start Date*: 2020-05-18 |
Sponsor Name:Pablo Rama Maceiras | ||
Full Title: Effectiveness comparative study of oblique subcostal transversus abdominis plane block (OSTAP block) versus laparoscopic ports infiltration in patients undergoing elective cholecystectomy. | ||
Medical condition: Elective cholecystectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002586-34 | Sponsor Protocol Number: STEROID_MC_1 | Start Date*: 2020-11-12 | |||||||||||||||||||||||||||||||
Sponsor Name:Department of Anesthesiology, Copenhagen University Hospital Hvidovre, Capital Region of Denmark | |||||||||||||||||||||||||||||||||
Full Title: The effects of preoperative high-dose Dexamethasone on inflammatory response and recovery after emergency laparotomy, a randomized, double-blind, placebo-controlled clinical trial - AHA STEROID ... | |||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing emergency laparotomy due to either Intestinal obstruction or perforated abdominal viscus. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001054-22 | Sponsor Protocol Number: OPMICS-1 | Start Date*: 2020-09-21 | |||||||||||
Sponsor Name:Claus Anders Bertelsen | |||||||||||||
Full Title: Laparoscopic vs Ultrasound-Guided Transversus Abdominis Plane Block in Minimally Invasive Colon Surgery: A Randomized Controlled Multicentre Clinical Trial | |||||||||||||
Medical condition: Colon cancer patients undergoing elective minimally invasive colon surgery and receiving a transversus abdominis plane block for postoperative pain management. Ropivacaine is used as the local anal... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000402-30 | Sponsor Protocol Number: SO_SH_01_2019 | Start Date*: 2019-04-10 | |||||||||||
Sponsor Name:Viktoria Lindberg-Larsen | |||||||||||||
Full Title: The effect of perioperative dexamethasone administration on postoperative pain in patients undergoing periacetabular osteotomy: A randomised double-blind, placebo-controlled trial | |||||||||||||
Medical condition: Dysplasia of the hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005928-13 | Sponsor Protocol Number: 52/2005 | Start Date*: Information not available in EudraCT |
Sponsor Name:Landspitali-University Hospital | ||
Full Title: Prospective randomized double blind trial on the use of Scopoderm patch for control of post-operative nausea and vomitting in patients undergoing gynecologic laparoscopic procedures. | ||
Medical condition: Post-operative nausea and vomiting in patients undergoing gynecologic laparoscopic procedures. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IS (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-003783-30 | Sponsor Protocol Number: EME-163-LOR-0025-I | Start Date*: 2005-04-27 |
Sponsor Name:Technical Unversity of Munich | ||
Full Title: Application of Aprepitant as salvage prophylaxis after failure of a conventional antiemetic therapy during moderately emetogenic chemotherapy in gastrointestinal cancer | ||
Medical condition: Chemotherapy-induced nasuea and vomiting (CINV) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-023297-39 | Sponsor Protocol Number: NETU-10-29 | Start Date*: 2011-05-27 | |||||||||||
Sponsor Name:Helsinn Healthcare SA | |||||||||||||
Full Title: A phase III, multicenter, randomized, double-blind, unbalanced (3:1) active control study to assess the safety and describe the efficacy of netupitant and palonosetron for the prevention of chemoth... | |||||||||||||
Medical condition: Nausea and vomiting in cancer patients associated with chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005515-10 | Sponsor Protocol Number: 0869-134 | Start Date*: 2009-01-22 | ||||||||||||||||
Sponsor Name:Merck & Co., Inc | ||||||||||||||||||
Full Title: "Estudio multicéntrico, abierto, de 5 partes para evaluar la farmacocinética, seguridad y tolerabilidad del aprepitant y de la dimeglumina de fosaprepitant en pacientes pediátricos que reciben quim... | ||||||||||||||||||
Medical condition: Nauseas y vómitos inducidos por quimioterapia Chemotherapy induced nausea and vomiting (CINV) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) SE (Completed) DE (Prematurely Ended) FR (Completed) Outside EU/EEA HU (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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