- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
48 result(s) found for: Groin.
Displaying page 1 of 3.
EudraCT Number: 2006-006234-18 | Sponsor Protocol Number: 15277 | Start Date*: 2007-03-26 |
Sponsor Name:Medisch Centrum Leeuwarden | ||
Full Title: Treatment of intertrigo: zinc oxide in ketoconazolecream with or without substitution of hydrocortisone | ||
Medical condition: Patients with intertrigo in the large skin folds as the groin, submammary and axillairy will be included for a medical trial. The intertrigo has to be two-sided, so each patient can be his own cont... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000988-25 | Sponsor Protocol Number: version4 | Start Date*: 2012-04-27 |
Sponsor Name:Gateshead Health NHS Trust Research & Development | ||
Full Title: To determine the feasibility of using Microbubble technology to detect sentinel nodes in vulvar cancer. | ||
Medical condition: Early stage vulvar cancer with no clinial or radiological evidence of lymph node metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000793-36 | Sponsor Protocol Number: HighNxGHR | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:Rigshospitalet, Copenhagen University Hospitals | |||||||||||||
Full Title: Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia in Patients following Groin-Hernia-Repair. A companion study to: Pharmacokinetics of High-dose Target-controlled Nal... | |||||||||||||
Medical condition: Groin hernia repair | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000875-20 | Sponsor Protocol Number: C3291028 | Start Date*: 2020-05-14 |
Sponsor Name:Pfizer Inc. | ||
Full Title: A Phase 2b, Multi Center, Randomized, Double-Blind, Vehicle-Controlled, Intra-Participant Study, to Evaluate Efficacy and Safety of Two Regimens of Crisaborole Ointment 2% in Japanese Pediatric and... | ||
Medical condition: Atopic Dermatitis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2020-001599-13 | Sponsor Protocol Number: TNKCAT | Start Date*: 2021-08-13 |
Sponsor Name:Hospital Vall Hebron | ||
Full Title: Tenecteplase Compared to Alteplase for Large Vesel Oclusion patients before Thrombectomy | ||
Medical condition: Acute Ischaemic Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001191-30 | Sponsor Protocol Number: IISR-2015-101127 | Start Date*: 2017-04-25 | |||||||||||
Sponsor Name:Department of Obstetrics & Gynecology, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Use of TachoSil® for the prevention of postoperative complications after groin dissection in vulva cancer patients | |||||||||||||
Medical condition: Vulva cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-006059-13 | Sponsor Protocol Number: Tacho01 | Start Date*: 2012-04-16 | |||||||||||
Sponsor Name:A.O. UNIVERSITARIA INTEGRATA DI VERONA | |||||||||||||
Full Title: The use of Tachosil as sealant in the prevention of lymphorrea after groin lymphadenectomy for vulvar cancer: a clinical controlled prospective trial | |||||||||||||
Medical condition: lymphedema after groin lymphadenectomy in patients with vulvar cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005482-10 | Sponsor Protocol Number: RN1001-0042 | Start Date*: 2006-03-13 |
Sponsor Name:Renovo | ||
Full Title: A double blind, placebo controlled, randomised dose response trial to investigate the efficacy of Juvista in the improvement of scar appearance when applied to approximated wound margins following ... | ||
Medical condition: Patients undergoing varicose vein removal with ligation and stripping. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) LT (Completed) LV (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000815-42 | Sponsor Protocol Number: HighNxGHR_PK | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:Rigshospitalet, Copenhagen University Hospitals | |||||||||||||
Full Title: Pharmacokinetics of High-dose Target-controlled Naloxone Infusion. Companion study to: Effect of High-dose Target-controlled Naloxone Infusion on Pain and Hyperalgesia in Patients following Groin-H... | |||||||||||||
Medical condition: Healthy subjects | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002741-39 | Sponsor Protocol Number: TIMELI001 | Start Date*: 2005-12-07 | |||||||||||
Sponsor Name:Prof. Giampiero CAMPANELLI | |||||||||||||
Full Title: A prospective, controlled, randomized, patient and evaluator blinded study to evaluate pain and further disabling complications in patients undergoing Lichtenstein technique for primary inguinal he... | |||||||||||||
Medical condition: Unilateral, uncomplicated primary inguinal hernia repair | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004725-40 | Sponsor Protocol Number: ECOBT | Start Date*: 2015-11-04 |
Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut MAR) | ||
Full Title: Interfascial effectiveness of ultrasound-guided blocking in transurethral resection of bladder tumor | ||
Medical condition: Bladder cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002412-23 | Sponsor Protocol Number: DUO2022_01 | Start Date*: 2022-12-30 |
Sponsor Name:MB PHARMA s. r. o. | ||
Full Title: A prospective, randomized, double-blind, placebo-controlled Phase I/IIA Clinical Trial to demonstrate the safety and efficacy of DUOFAG® in bacterial infection treatment in patients with surgical w... | ||
Medical condition: Bacterial infection with Staphylococcus aureus and/or Pseudomonas aeruginosa in the surgical wound. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000435-13 | Sponsor Protocol Number: JWGKDVAAP0117 | Start Date*: 2017-11-13 |
Sponsor Name:University Hospital Frankfurt for its Dermatology Department, Clinical Research | ||
Full Title: Exploratory study to evaluate changes in inflammatory pattern and analysis for serum biomarkers in patients with active, moderate-to-severe hidradenitis suppurativa after 2-week and 6-week treatmen... | ||
Medical condition: Hidradenitis suppurativa is defined as a chronic inflammatory disease of the intertriginous area, including the axilla, groin and anogenital or submammary regions. The condition is characterized by... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019899-77 | Sponsor Protocol Number: dx3 | Start Date*: 2010-06-21 | ||||||||||||||||||||||||||
Sponsor Name:Mette Astrup Madsen | ||||||||||||||||||||||||||||
Full Title: Can preoperative Dexamethasone optimise surgical outcomes after laparoscopic inguinal hernia repair. | ||||||||||||||||||||||||||||
Medical condition: Postoperative pain, nausea, vomiting, general well-being and convalescence after laparoscopic groin hernia repair. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004052-20 | Sponsor Protocol Number: CKTO 2005-25R | Start Date*: 2006-11-01 | |||||||||||
Sponsor Name:Koningin Wilhelmina Fonds | |||||||||||||
Full Title: Phase II study of definitive radiochemotherapy for locally advanced squamous cell cancer of the vulva: an efficacy study | |||||||||||||
Medical condition: advanced stage squamous cell cancer of the vulva | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002692-98 | Sponsor Protocol Number: GH001 | Start Date*: 2017-10-04 | |||||||||||
Sponsor Name:GAMA Healthcare | |||||||||||||
Full Title: An evaluation of the efficacy of HEXI-PREP by Clinell Wipes versus placebo and ChloraPrep, for use in pre-operative skin preparation | |||||||||||||
Medical condition: For disinfection of the skin, immediately prior to invasive medical procedures | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003845-40 | Sponsor Protocol Number: 122-0551-209 | Start Date*: 2019-07-09 | |||||||||||
Sponsor Name:Mayne Pharma LLC | |||||||||||||
Full Title: An open label evaluation of the adrenal suppression potential and pharmacokinetic properties of twice daily halobetasol propionate foam, 0.05% in subjects 12 to less than 18 years of age with plaqu... | |||||||||||||
Medical condition: Plaque psoriasis | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001982-36 | Sponsor Protocol Number: AcT_CZE | Start Date*: 2020-08-19 | ||||||||||||||||
Sponsor Name:FakultnĂ nemocnice u sv. Anny | ||||||||||||||||||
Full Title: Alteplase compared to tenecteplase in patients with acute ischemic stroke: Registry-based pragmatic randomized controlled trial | ||||||||||||||||||
Medical condition: Acute ischemic stroke | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003973-16 | Sponsor Protocol Number: 2016-00601 | Start Date*: 2020-11-02 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Groningen International Study on Sentinel nodes in Vulvar cancer - III, a prospective phase 2 treatment trial | ||
Medical condition: vulvar cancer patients with sentinel lymph node metastases larger than 2mm | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-004179-42 | Sponsor Protocol Number: HS0005 | Start Date*: 2021-07-06 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Phase 3, Open-Label, Parallel Group, Multicenter, Extension Study Evaluating the Long-Term Treatment of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis Suppurativa | |||||||||||||
Medical condition: Hidradenitis Suppurativa | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Ongoing) CZ (Ongoing) GR (Ongoing) HU (Completed) BG (Ongoing) BE (Completed) IT (Ongoing) NL (Ongoing) DK (Completed) | |||||||||||||
Trial results: (No results available) |
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