- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (70)
69 result(s) found for: gabapentin.
Displaying page 1 of 4.
EudraCT Number: 2016-002177-35 | Sponsor Protocol Number: GNB-2015 | Start Date*: 2018-05-07 |
Sponsor Name:Masarykova univerzita | ||
Full Title: The effect of gabapentin used as a preemptive to the emergence and development chronic neuropathic pain in patients after spinal cord trauma | ||
Medical condition: Chronic neuropathic pain in patients after spinal cord trauma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005494-22 | Sponsor Protocol Number: | Start Date*: 2012-06-21 | |||||||||||
Sponsor Name:University of Edinburgh [...] | |||||||||||||
Full Title: GaPP: A pilot randomised controlled trial of the efficacy and mechanism of action of gabapentin for the management of chronic pelvic pain in women | |||||||||||||
Medical condition: Chronic pelvic pain | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010783-41 | Sponsor Protocol Number: GBPPKPD-09 | Start Date*: 2009-07-06 | |||||||||||
Sponsor Name:Uppsala University | |||||||||||||
Full Title: Population pharmacokinetic and pharmacodynamic modeling of gabapentin in neuropathic pain - Effect of adjuvant pharmacotherapy | |||||||||||||
Medical condition: Post-traumatic neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004837-33 | Sponsor Protocol Number: A9451046 | Start Date*: 2005-04-11 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: A randomised, double-blind, parallel group trial to assess the variability and treatment effect size for a Neuropathic Pain offset design | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004791-39 | Sponsor Protocol Number: 57019085 | Start Date*: 2008-04-22 |
Sponsor Name:Vejle Hospital | ||
Full Title: Et prospektivt randomiseret fase II studie til evaluering af Gabapentin og Venlafaxin´s virkning mod hedestigninger hos kvinder opereret for brystkræft og i antihormonbehandling i form af arom... | ||
Medical condition: Patients in adjuvant aromatase inhibitor treatment for breast cancer having serious side effects conserning hot flashes affecting daily life. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013036-20 | Sponsor Protocol Number: 2009292 | Start Date*: 2009-10-15 |
Sponsor Name:Rigshospital | ||
Full Title: Effekten af Gabapentin på urin kateter gener hos patienter med et abdominalt aorta aneurisme som behandles med en endovaskulær stent | ||
Medical condition: Patienter med et infrarenalt abdominalt aorta aneurisme (AAA) >18 år. KAD i den tidlige postoperative periode medføre smerter/gener med øgning af som opleves værre end smerter sekundært til operati... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005996-32 | Sponsor Protocol Number: LDH0230 | Start Date*: 2008-06-25 |
Sponsor Name:Luton & Dunstable Hospital NHS Foundation Trust | ||
Full Title: To determine the pre-emptive effect of Gabapentin on acute and chronic post-operative pain after spinal surgery | ||
Medical condition: Acute and chronic back pain after surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000133-12 | Sponsor Protocol Number: 039(1)PO16357 | Start Date*: 2018-10-26 | |||||||||||||||||||||
Sponsor Name:Angelini S.p.A. | |||||||||||||||||||||||
Full Title: Efficacy and safety of Fixed-Dose Combination (FDC) products containing trazodone and gabapentin in patients affected by painful diabetic neuropathy: randomized, controlled, dose finding study. | |||||||||||||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) GB (Completed) PL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-004174-42 | Sponsor Protocol Number: A9451162 | Start Date*: 2015-04-06 |
Sponsor Name:Pfizer Japan Inc. | ||
Full Title: An Open-Label, Multicenter Study Evaluating, The Efficacy, Safety And Pharmacokinetics Of Gabapentin As Adjunctive Therapy In Pediatric Subjects With Partial Seizures When Other Antiepileptics Do N... | ||
Medical condition: Epilepsy with partial seizures (including secondarily generalized seizures) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2007-004297-40 | Sponsor Protocol Number: Version 3 February 2010 | Start Date*: 2008-04-25 |
Sponsor Name:University Hospitals of Leicester NHS Trust | ||
Full Title: Pharmacological treatment of nystagmus: A randomised double masked placebo controlled crossover study using gabapentin and memantine. | ||
Medical condition: Nystagmus | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004933-99 | Sponsor Protocol Number: PXN110527 | Start Date*: 2008-10-23 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: Study PXN110527: The investigation of the efficacy and pharmacokinetics of XP13512 in subjects with neuropathic pain associated with post-herpetic neuralgia (PHN) who have had an inadequate respons... | |||||||||||||
Medical condition: Neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004175-23 | Sponsor Protocol Number: A9451165 | Start Date*: 2015-04-07 |
Sponsor Name:Pfizer Japan Inc | ||
Full Title: A 52 weeks, open-label, multicenter study evaluating the efficacy and safety of gabapentin as adjunctive therapy in pediatric subjects who have completed the 12 weeks treatment in study A9451162. | ||
Medical condition: Epilepsy with partial seizures (including secondarily generalized seizures) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-010437-50 | Sponsor Protocol Number: GABAPRURE01/09 | Start Date*: 2009-04-02 |
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE S. MARIA NUOVA | ||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY OF DIFFERENT GABAPENTIN DOSES IN HAEMODIALYSIS PATIENTS WITH UREMIC PRURITUS. | ||
Medical condition: Haemodialysis subjects with uremic itch. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002078-38 | Sponsor Protocol Number: SU/2016/6033 | Start Date*: 2017-12-06 | |||||||||||||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Effectiveness, cost effectiveness and safety of gabapentin versus placebo as an adjunct to multimodal pain regimens in surgical patients: A placebo controlled randomised controlled trial with blind... | |||||||||||||||||||||||
Medical condition: Post surgery pain management | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000521-31 | Sponsor Protocol Number: PI12_01813 | Start Date*: 2013-12-26 | |||||||||||
Sponsor Name:Gerencia de Atención Primaria de Mallorca | |||||||||||||
Full Title: Efficacy and safety of gabapentin versus placebo to prevent the incidence of PostHerpetic Neuralgia | |||||||||||||
Medical condition: Postherpetic Neuralgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004851-30 | Sponsor Protocol Number: GABA-1 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:PHARM – Pharmaceutical Research Management srl | |||||||||||||
Full Title: Randomized, double-blind, double-dummy, active controlled, multicentre, non-inferiority phase-III study to compare the pharmacokinetic, efficacy and safety of gabapentin liquid formulation to trama... | |||||||||||||
Medical condition: Chronic pain of neuropathic or mixed origin | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) DE (Completed) FR (Ongoing) GR (Prematurely Ended) GB (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001165-33 | Sponsor Protocol Number: ML2676 | Start Date*: 2005-04-26 |
Sponsor Name:Bart Morlion | ||
Full Title: A prospective, open randomized, parallel group trial to compare the efficacy and safety of transdermal buprenorphine (Transtec) with gabapentin (Neurontin) in patients with neuropatic pain syndromes | ||
Medical condition: Neuropathic pain | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004897-40 | Sponsor Protocol Number: GABA-2 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:PHARM – Pharmaceutical Research Management srl | |||||||||||||
Full Title: Randomized, double-blind, placebo controlled, multi-centre, superiority phase II study to evaluate the safety, pharmacokinetic, efficacy of gabapentin liquid formulation as add-on to morphine in ch... | |||||||||||||
Medical condition: Chronic pain of neuropathic or mixed origin | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) FR (Ongoing) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003595-38 | Sponsor Protocol Number: OMA-AH01 | Start Date*: 2005-12-07 |
Sponsor Name:Dept of Anaesthesiology 530 | ||
Full Title: Optimeret multimodal analgesi ved abdominal hysterectomi | ||
Medical condition: Elektiv, åben operation for fjernelse af livmoder (abdominal hysterectomi) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002769-11 | Sponsor Protocol Number: Gabapentin02 | Start Date*: 2010-01-25 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of Cardiothoracic and Vascular Surgery | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: THE EFFECT OF GABAPENTIN ON THORACIC EPIDURAL ANALGESIA FOLLOWING THORACOTOMY – A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: The purpose of this trial is to investigate the effect of gabapentin on thoracic epidural analgesia following thoracotomy, including assessment of both analgesia, pain intensity, pain quality and w... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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