- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Abdominoplasty.
Displaying page 1 of 1.
EudraCT Number: 2016-002538-58 | Sponsor Protocol Number: BS-AIO-2015-QL-block | Start Date*: 2016-10-04 |
Sponsor Name:Avdeling for Anestesi, Intensiv og Operasjon Bærum Sykehus | ||
Full Title: QUADRATUS LUMBORUM BLOCK FOR PERIOPERATIVE ANALGESIA IN PATIENTS TREATED WITH ABDOMINOPLASTY. A RANDOMISED CONTROLLED TRIAL | ||
Medical condition: postbariatric abdominoplasty | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004353-24 | Sponsor Protocol Number: WMPS | Start Date*: 2014-05-07 | |||||||||||||||||||||
Sponsor Name:Universität Leipzig | |||||||||||||||||||||||
Full Title: Wound Management in Post-Bariatric Surgery Investigation for the reduction of the mean drainage volume in patients after abdominoplasty / lower body lift using Artiss Fibrin Sealant in comparison t... | |||||||||||||||||||||||
Medical condition: Post-bariatric surgery, abdominoplasty, lower body lift | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000626-29 | Sponsor Protocol Number: KS001 | Start Date*: 2011-12-13 |
Sponsor Name:QUEEN MARY UNIVERSITY OF LONDON | ||
Full Title: Keloid Scars: A randomised clinical and laboratory based study on the treatment and differentiation factors of the local disease | ||
Medical condition: Keloid scarring | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010173-20 | Sponsor Protocol Number: A3051113 | Start Date*: 2009-08-06 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
Full Title: A MULTICENTER, OPEN LABEL STUDY TO INVESTIGATE THE FEASIBILITY AND EFFICACY OF A SMOKING CESSATION PROGRAM WITH VARENICLINE IN PATIENTS UNDERGOING ELECTIVE SURGERY | |||||||||||||
Medical condition: Smoking cessation in patients scheduled for elective surgery. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006174-47 | Sponsor Protocol Number: FC-004 | Start Date*: 2012-06-08 | |||||||||||
Sponsor Name:ProFibrix BV | |||||||||||||
Full Title: A Phase 3, Randomized, Single-Blind, Controlled Trial of Topical Fibrocaps™ in Intraoperative Surgical Haemostasis | |||||||||||||
Medical condition: Intraoperative Surgical Hemostasis (Spinal Surgery, Vascular Surgery, Hepatic resection, Soft tissue dissection) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) GB (Completed) | |||||||||||||
Trial results: Removed from public view |
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