- Trials with a EudraCT protocol (7)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
7 result(s) found for: Spinal needle.
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EudraCT Number: 2013-004013-41 | Sponsor Protocol Number: AUH-TFB-SSPS-3 | Start Date*: 2015-09-18 | ||||||||||||||||
Sponsor Name:Thomas Fichnter Bendtsen | ||||||||||||||||||
Full Title: Supra Sacral Parallel Shift - ultrasound/MR image fusion guided lumbosacral plexus block | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002179-12 | Sponsor Protocol Number: PRILODE50-FUSION | Start Date*: 2022-09-16 | |||||||||||
Sponsor Name:Matilde Zaballos | |||||||||||||
Full Title: Determination of the effective dose 50 of intrathecal hyperbaric prilocaine required for the transrectal ultrasound guidance fusion-targeted prostate biopsy in ambulatory surgery | |||||||||||||
Medical condition: anaesthesia for prostate fusion biopsy in outpatient surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005544-33 | Sponsor Protocol Number: AUH-TFB-SR-ULMR | Start Date*: 2016-02-08 | ||||||||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | ||||||||||||||||||
Full Title: Shamrock – Ultrasound/MR image fusion guided lumbar plexus blocks | ||||||||||||||||||
Medical condition: Hip surgery anaesthesia and perioperative analgesia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-005019-15 | Sponsor Protocol Number: CCTL019C2202 | Start Date*: 2018-11-08 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A Phase II, single arm, multicenter open label trial to determine the safety and efficacy of tisagenlecleucel in pediatric patients with relapsed or refractory mature B-cell non-Hodgkin lymphoma (N... | |||||||||||||
Medical condition: pediatric and adolescents patients with CD19positive r/r mature B-cell NHL who have relapsed after one or more prior therapies or are primary refractory. | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Completed) DE (Completed) SE (Ongoing) DK (Completed) NO (Completed) AT (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005069-30 | Sponsor Protocol Number: UG1_2016 | Start Date*: 2017-02-28 | |||||||||||
Sponsor Name:Pia Jæger | |||||||||||||
Full Title: Comparison of the analgesic effect of an adductor canal block using a new suture-method catheter vs a standard perineural catheter vs a single bolus: A randomized, blinded, controlled study | |||||||||||||
Medical condition: Primary total knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000317-17 | Sponsor Protocol Number: ICI20-00047 | Start Date*: 2021-08-11 | |||||||||||
Sponsor Name:Fundación para la Gestión de la Investigación Biomédica de Cádiz-INIBICA | |||||||||||||
Full Title: Survival analysis after neoadjuvant therapy in patients with resectable pancreatic cancer and risk factors | |||||||||||||
Medical condition: Resectable pancreatic cancer and risk factors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005180-40 | Sponsor Protocol Number: Protocol_PPB_TKA_31122017 | Start Date*: 2018-02-19 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: The effect of the popliteal plexus block on postoperative pain after total knee arthroplasty - a randomized, controlled, double-blinded study | |||||||||||||||||||||||
Medical condition: Postoperative posterior pain after total knee arthroplasty | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
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