- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
55 result(s) found for: Suture.
Displaying page 1 of 3.
EudraCT Number: 2005-000869-20 | Sponsor Protocol Number: DC0071-BB-404-8B | Start Date*: 2005-08-08 |
Sponsor Name:Pierre Fabre Médicament | ||
Full Title: Post-operative care by chlorhexidine mouthwash after periodontal surgery. Randomised, parallel groups; blind study, DC071BB versus placebo, in patients presenting with periodontal surgery with sutu... | ||
Medical condition: Post-operative care for patients having periodontal surgery with gingival suture. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) EE (Completed) LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-003558-26 | Sponsor Protocol Number: BIOS-13-006 | Start Date*: 2014-07-21 |
Sponsor Name:Ethicon Inc | ||
Full Title: A Prospective, Randomized, Controlled, Study Evaluating the Safety and Efficacy of EVICEL® used for Suture-line sealing in Dura-Mater Closure during Paediatric Neurosurgical Cranial Procedures | ||
Medical condition: Subjects undergoing neurosurgical cranial procedures, requiring water-tight closures (suture-line sealing) in dura-mater during the surgery | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2012-002704-41 | Sponsor Protocol Number: SM2-UG12 | Start Date*: 2012-09-18 |
Sponsor Name:Rigshospitalet | ||
Full Title: Effect of Adductor-Canal-Blockade on postoperative pain, ability to walk and morphine consumption after total knee arthroplasty: A randomised study | ||
Medical condition: Treatment of postoperative pain in patients after total knee arthroplasty | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001056-35 | Sponsor Protocol Number: TXA | Start Date*: 2014-11-24 | |||||||||||
Sponsor Name:IRCCS Istituto Giannina Gaslini | |||||||||||||
Full Title: The Effectiveness and Population Pharmacokinetics and Pharmacogenomics of a Reduced Dose of Tranexamic Acid for Craniosynostosis Surgery: A multicenter study. The TXA Study. | |||||||||||||
Medical condition: craniosynostosis | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000545-22 | Sponsor Protocol Number: 2012/462. | Start Date*: 2015-08-05 | |||||||||||
Sponsor Name:Aarhus University hospital | |||||||||||||
Full Title: Effects of Tranexamic Acid on on Intra- and Postoperative bleeding, Blood transfusion and Coagulation in Children Undergoing Craniosynostosis Surgery | |||||||||||||
Medical condition: Bleeding during paediatric Craniosynostosis surgery | |||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000242-17 | Sponsor Protocol Number: Protocol_PPB_TKA_14012021 | Start Date*: 2021-03-12 | |||||||||||
Sponsor Name:Region Hospital Silkeborg | |||||||||||||
Full Title: The effect of the popliteal plexus block on postoperative opioid consumption, pain, muscle strength and mobilization after total knee arthroplasty - a randomized, controlled, blinded study | |||||||||||||
Medical condition: Postoperative pain following a total knee arthroplasty surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003409-98 | Sponsor Protocol Number: HERA-05/001 | Start Date*: 2006-02-09 |
Sponsor Name:Hôpital Erasme, Cliniques Universitaires de Bruxelles | ||
Full Title: Enhancement by tacrolimus of nerve regeneration after peripheral nerve repair. | ||
Medical condition: Patients presenting a total section of a major nerve at the arm, forearm, or leg, and treated by conventional nerve suture under microscope within ten days of the trauma. Patients with nerve autogr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003464-31 | Sponsor Protocol Number: BIOS-13-004 | Start Date*: 2014-02-21 |
Sponsor Name:Ethicon Inc | ||
Full Title: A Single-blinded, Randomized, Controlled, Comparative Phase III Study Evaluating the Safety and Effectiveness of EVARREST™ Fibrin Sealant Patch as an Adjunct to Hemostasis During Cardiovascular Sur... | ||
Medical condition: subjects undergoing major aortic surgery, including ascending, arch, or descending aorta replacement, requiring adjunctive support for hemostasis at the anastomotic suture line | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016501-41 | Sponsor Protocol Number: 400-09-001 | Start Date*: 2010-06-29 |
Sponsor Name:Omrix Biopharmaceuticals Ltd | ||
Full Title: A Randomized, Controlled Study to Evaluate the Safety and Effectiveness of Evicel as an Adjunct to Sutured Dural Repair | ||
Medical condition: tissue adhesion/sealing and suture support in neurosurgery and surgical procedures where contact with cerebrospinal fluid or dura mater can occur e.g. otologic, rhinologic, ophthalmic and vertebral... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) NL (Completed) FI (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002802-19 | Sponsor Protocol Number: NMBDKHernia2014 | Start Date*: 2014-09-19 | |||||||||||
Sponsor Name:Department of Anaesthesiology | |||||||||||||
Full Title: Optimizing surgical conditions during laparoscopic umbilical, incisional –and linea alba herniotomy with deep neuromuscular blockade (The hernia study) | |||||||||||||
Medical condition: The purpose of this study is to investigate surgical work space and surgical conditions in patients scheduled for laparoscopic umbilical, -linea alba and incisional herniotomy. The patients will ac... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005856-42 | Sponsor Protocol Number: NKT102553 | Start Date*: 2006-03-29 |
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
Full Title: A Phase III, Multicenter, Randomized, Double-blind, Parallel Group Study to Evaluate the Safety and Efficacy of 50 mg Oral Dosing with the Neurokinin-1 Receptor Antagonist GW679769 for the Preventi... | ||
Medical condition: Postoperative Nausea and Vomiting (PONV) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) HU (Completed) DE (Completed) IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005855-16 | Sponsor Protocol Number: NKT102552 | Start Date*: 2006-03-20 |
Sponsor Name:GlaxoSmithKline Research and Development Ltd | ||
Full Title: A Phase III Multicenter, Randomized, Double-blind, Parallel Group Study to Evaluate the Safety and Efficacy of the 30 mg Intravenous Formulation of the Neurokinin-1 Receptor Antagonist GW679769 for... | ||
Medical condition: Postoperative Nausea and Vomiting (PONV) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) HU (Completed) ES (Completed) CZ (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002952-34 | Sponsor Protocol Number: ACH-UCP-301 | Start Date*: 2015-12-07 | |||||||||||
Sponsor Name:Atlantic Pharmaceuticals Limited | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled Trial of the Safety and Efficacy of Topical Alicaforsen Enema in Subjects with Active, Chronic, Antibiotic Refractory Primary Idiopathic Pouchitis | |||||||||||||
Medical condition: Active, Chronic, Antibiotic Refractory Primary Idiopathic Pouchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) IE (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004565-24 | Sponsor Protocol Number: CNS7056-011 | Start Date*: 2015-06-22 | |||||||||||
Sponsor Name:PAION UK Limited | |||||||||||||
Full Title: A Randomized, Single-blind, Propofol-controlled Phase III Study Evaluating the Efficacy and Safety of Remimazolam in General Anesthesia in Adult Patients Undergoing Cardiac Surgery, Including Follo... | |||||||||||||
Medical condition: Anesthesia in adult patients undergoing cardiac surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001778-12 | Sponsor Protocol Number: HUGTP-CIR-FIBRIN-GLUE-01 | Start Date*: 2019-04-15 | |||||||||||||||||||||
Sponsor Name:Fundació Institut de Recerca en Ciències de la Salut Germans Trias i Pujol | |||||||||||||||||||||||
Full Title: USE OF A FIBRINE ADHESIVE TO REDUCE THE DEHISCENCE OF ESOFAGOYEYUNAL ANASTOMOSIS IN TOTAL GASTRECTOMIES BY CANCER: RANDOMIZED AND MULTICENTRIC STUDY. | |||||||||||||||||||||||
Medical condition: The dehiscence of the esophagojejunal anastomosis after a total gastrectomy in patients with gastric adenocarcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002517-20 | Sponsor Protocol Number: SM2-05 | Start Date*: 2005-08-01 |
Sponsor Name:Dept. of Anaestesiology, University hospital in Glostrup | ||
Full Title: Effect of paracetamol, low dose Ketamin, paracetamol, NSaid and dexametason on pain and opioid requirements in patients scheduled for primary total hip replacement | ||
Medical condition: Patient scheduled for primary total hip replacement need postoperativ pain treatment. Morphine has side-effects: nause, vomiting, sedation and dizziness. These sideeffects are of course unpleasent ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001093-16 | Sponsor Protocol Number: DX203 | Start Date*: 2013-07-16 |
Sponsor Name:Oculis ehf. | ||
Full Title: Comparison of non-MMC trabeculectomy and dexamethasone nanoparticles eye drops with MMC trabeculectomy and Maxidex® | ||
Medical condition: Anti-inflammatory treatment post trabeculectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006001-16 | Sponsor Protocol Number: HVF-001-2008 | Start Date*: 2008-12-10 | |||||||||||
Sponsor Name:AZIENDA UNITA` SANITARIA LOCALE LECCE | |||||||||||||
Full Title: Efficacy of TachoSil on air leakage in chest surgery | |||||||||||||
Medical condition: Patient undergone lobectomy or segmentectomy (anatomical segmentectomy) for lung carcinoma and that during intraoperative phase after first suture with stapler show air leakage with grade 1-2 accor... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003151-11 | Sponsor Protocol Number: CNTO1275UCO2001 | Start Date*: 2020-05-08 |
Sponsor Name:UZ Leuven | ||
Full Title: Stelara fOr ChRonic AntibioTic rEfractory pouchitiS (SOCRATES): A Belgian open label multicenter pilot-study | ||
Medical condition: Chronic antibiotic refractory and relapsing pouchitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004738-14 | Sponsor Protocol Number: NanoGSkin-CB-2019 | Start Date*: 2020-04-28 | ||||||||||||||||
Sponsor Name:Red Andaluza de Diseño y Traslación de Terapias Avanzadas - Fundación Pública Andaluza Progreso y Salud | ||||||||||||||||||
Full Title: PHASE II CLINICAL TRIAL EVALUATING THE SAFETY AND EFFICACY OF A TISSUE ENGINEERED AUTOLOGOUS SKIN SUBSTITUTE RECONSTRUCTIVE SURGERY FOR BASAL CELL CARCINOMA. | ||||||||||||||||||
Medical condition: Reconstructive skin surgery in basal cell cancer (Mohs surgery) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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