- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
9 result(s) found for: Oblique.
Displaying page 1 of 1.
| EudraCT Number: 2008-005657-38 | Sponsor Protocol Number: TAPprotocol12008 | Start Date*: 2008-11-18 | |||||||||||
| Sponsor Name:Royal College of Surgeons Ireland | |||||||||||||
| Full Title: Transversus Abdominis Plane Block for Analgesia in Renal Transplantation: A Randomised Controlled Trial | |||||||||||||
| Medical condition: Condition to be investigated - Analgesia requirements in patients having renal transplant surgery. The study proposes to reduce current requirements for morphine post-operatively by the use of a T... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (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: 2009-015939-33 | Sponsor Protocol Number: 20080394 | Start Date*: 2010-03-23 |
| Sponsor Name:Amgen Inc | ||
| Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Study to Determine the Efficacy, Safety, and Tolerability of AMG 785 in Adults with Fresh Unilateral Intertrochanteric Fracture of the P... | ||
| Medical condition: Acceleration of fracture healing | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: FR (Completed) GB (Completed) DE (Completed) SE (Completed) PL (Completed) DK (Completed) NL (Completed) LV (Completed) GR (Completed) IT (Completed) HU (Completed) BE (Completed) FI (Completed) LT (Completed) EE (Completed) BG (Completed) SI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-000157-23 | Sponsor Protocol Number: version1.1SFINX | Start Date*: 2011-09-27 |
| Sponsor Name:UMC St Radboud | ||
| Full Title: Street Fitness In surgical patieNts undergoing general anesthesia after reversal of neuromuscular rest blockade with sugammadeX (SFINX study) | ||
| Medical condition: Males and females in the age of 18-65 undergoing minor surgery/gynaecological procedures with a medical need for general anesthesia and neuromuscular blockade will be included in the study. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004053-20 | Sponsor Protocol Number: TAP3 | Start Date*: 2006-12-08 | |||||||||||
| Sponsor Name:Dept of Anaesthesia, University College Hospital, Galway | |||||||||||||
| Full Title: Determination of the efficacy of the Transversus Abdominis Plane (TAP) Block in the management of postoperative pain following Caesarean Section. | |||||||||||||
| Medical condition: Post operative pain | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004049-41 | Sponsor Protocol Number: TAP2 | Start Date*: 2006-12-08 | |||||||||||
| Sponsor Name:Dept of Anaesthesia, University College Hospital, Galway | |||||||||||||
| Full Title: Determination of the efficacy of the Transversus Abdominis Plane (TAP) Block in the management of postoperative pain following Total Abdominal Hysterectomy (TAH). | |||||||||||||
| Medical condition: Post operative pain following Total Abdominal Hysterectomy. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004034-11 | Sponsor Protocol Number: GR-OG-279239-04 | Start Date*: 2022-05-18 | ||||||||||||||||
| Sponsor Name:Genera Research Ltd | ||||||||||||||||||
| Full Title: A randomized, evaluator-blinded, dose-ranging, proof of concept study of efficacy, safety and tolerability of Osteogrow-C (rhBMP6 delivered in autologous blood coagulum [ABC] supplemented with sy... | ||||||||||||||||||
| Medical condition: The treatment of non-union of the tibia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-004377-41 | Sponsor Protocol Number: TFP_1-1 | Start Date*: 2016-12-19 | |||||||||||
| Sponsor Name:Dep. Anaesthesia and Intensive Care, Aarhus University Hospital | |||||||||||||
| Full Title: Regional anaesthesia of the cutaneus nerves of the hip - A randomized controlled trial of the transversalis fascia plane block | |||||||||||||
| Medical condition: Postoperative pain after hip surgery | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-001755-41 | Sponsor Protocol Number: GV971-007 | Start Date*: 2021-02-10 | |||||||||||
| Sponsor Name:Green Valley (Shanghai) Pharmaceuticals Co., Ltd. | |||||||||||||
| Full Title: A Phase 3, multi-center, randomized, double-blind, parallel-group, placebo-controlled clinical trial to evaluate the efficacy and safety of sodium oligomannate (GV-971) in treatment of mild to mode... | |||||||||||||
| Medical condition: mild to moderate Alzheimer’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) DE (Prematurely Ended) FR (Prematurely Ended) PL (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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