- Trials with a EudraCT protocol (148)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
148 result(s) found for: Digestive System Diseases AND Pain AND Placebo.
Displaying page 1 of 8.
EudraCT Number: 2014-005467-32 | Sponsor Protocol Number: n.a. | Start Date*: 2016-08-08 |
Sponsor Name:Haga Teaching Hospital | ||
Full Title: A randomised controlled trial on the effect of laxative therapy in children with functional abdominal pain | ||
Medical condition: Functional abdominal pain | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003690-65 | Sponsor Protocol Number: 78304 | Start Date*: 2021-11-10 |
Sponsor Name:St Antonius Hospital | ||
Full Title: Peppermint Oil for the treatment of Irritable Bowel Syndrome or Functional Abdominal Pain in Children: the MINT study | ||
Medical condition: Irritable Bowel syndrome Functional Abdominal Pain Not otherwise specified | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005060-26 | Sponsor Protocol Number: ONU3704 | Start Date*: 2012-06-19 | ||||||||||||||||
Sponsor Name:Purdue Pharma L.P. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Double-dummy, Placebo-controlled, Active-controlled, Parallel-group, Multicenter Trial of Oxycodone/Naloxone Controlled-release Tablets (OXN) to Assess the Analgesic Eff... | ||||||||||||||||||
Medical condition: Opioid-induced Constipation & Moderate to Severe Chronic Low back Pain | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003293-32 | Sponsor Protocol Number: Duski2015 | Start Date*: 2017-11-06 | ||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||
Full Title: Multicentre, Randomised, Placebo-Controlled Trial of Mebeverine in Children with Irritable Bowel Syndrome (IBS) or Functional Abdominal Pain - not otherwise specified (FAP-NOS) | ||||||||||||||||||
Medical condition: Functional Gastrointestinal Disorders (Irritable Bowel Syndrome or Functional Abdominal Pain - not otherwise specified) | ||||||||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002110-42 | Sponsor Protocol Number: PHRCIR2015DAPOIGNY | Start Date*: 2017-10-18 |
Sponsor Name:CHU CLERMONT-FERRAND | ||
Full Title: Evaluation of the effectiveness and safety of ethosuximide in the treatment of abdominal pain associated with irritable bowel syndrome | ||
Medical condition: abdominal pain related to irritable bowel syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004354-28 | Sponsor Protocol Number: S-20120017 | Start Date*: 2013-07-02 |
Sponsor Name:Børneafdelingen Kolding | ||
Full Title: Maintenance treatment in childhood constipation. A randomized placebo-controlled intervention study | ||
Medical condition: Childhood functional constipation. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003466-25 | Sponsor Protocol Number: 13.024 | Start Date*: 2014-12-18 | |||||||||||
Sponsor Name:Anders Gadegaard Jensen,Anesthesia and Intensive Care Unit, Odense University Hospital | |||||||||||||
Full Title: Randomized, double-blind, prospective, placebo-controlled trial of the effect of intravenous lidocaine infusion for postoperative pain management and bowel function in robot assisted laparoscopic c... | |||||||||||||
Medical condition: Postoperative pain after colon rectal cancer surgery are mainly intended to relieve as well resting as activity-induced pain. Secondarily, the choice of pain management should take into considerati... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003357-17 | Sponsor Protocol Number: Ketamin_SST01 | Start Date*: 2013-11-01 | ||||||||||||||||
Sponsor Name:Prof. Asbjørn Mohr Drewes | ||||||||||||||||||
Full Title: RESET Trial A randomized, double-blinded, single-centre, parallel-group, placebo-controlled, prospective trial of S-ketamine for pain treatment in chronic pancreatitis (RESET trial) | ||||||||||||||||||
Medical condition: Chronic Pancreatitis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020906-14 | Sponsor Protocol Number: 50591903 | Start Date*: 2011-03-31 |
Sponsor Name:MUMC | ||
Full Title: Randomized controlled trial of escitalopram versus placebo for patients with irritable bowel syndrome and panic disorder. | ||
Medical condition: IBS and panic disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021604-16 | Sponsor Protocol Number: etoricoxib-fast-track-2010 | Start Date*: 2010-12-08 | |||||||||||
Sponsor Name:Charité Universitätsmedizin Berlin | |||||||||||||
Full Title: A double-blind, randomized, placebo controlled study to evaluate the effectiveness of etoricoxib as an additive analgesic to epidural analgesia in colon or rectum fast-track surgery | |||||||||||||
Medical condition: Post-operative pain after laparoscopic colon or rectum surgery in fast-track design | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004519-31 | Sponsor Protocol Number: ENTERL08784 | Start Date*: 2019-01-31 | |||||||||||
Sponsor Name:Sanofi | |||||||||||||
Full Title: Randomized, placebo-controlled, clinical trial to evaluate the efficacy of probiotic Bacillus clausii in the treatment of pediatric patients with irritable bowel syndrome | |||||||||||||
Medical condition: Irritable bowel syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003245-29 | Sponsor Protocol Number: SA652013 | Start Date*: 2016-12-19 |
Sponsor Name:Amsterdam AMC, locatie AMC | ||
Full Title: Ursodeoxycholic acid for the prevention of symptomatic gallstone disease after Roux-en-Y gastric bypass and Sleeve Gastrectomy | ||
Medical condition: Prevention of symptomatic gallstone disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014441-93 | Sponsor Protocol Number: X-03030-3277 | Start Date*: 2010-08-16 | |||||||||||
Sponsor Name:MEDA Pharma GmbH & Co. KG | |||||||||||||
Full Title: Clinical trial to assess the efficacy of the fixed combination product Tepilta® in the treatment of radiation-induced oesophagitis compared to its active ingredients oxetacaine and antacids, and t... | |||||||||||||
Medical condition: Radiation-induced oesophagitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005467-16 | Sponsor Protocol Number: 55995 | Start Date*: 2016-06-01 |
Sponsor Name:Maastricht University | ||
Full Title: Peppermint oil for the treatment of Irritable Bowel Syndrome: optimizing therapeutic strategies using targeted delivery | ||
Medical condition: Irritable Bowel Syndrome | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004626-28 | Sponsor Protocol Number: SymSF2 | Start Date*: 2019-07-18 |
Sponsor Name:SymbioPharm GmbH | ||
Full Title: Randomized, double-blind, placebo-controlled, multi-centre trial to evaluate the efficacy, safety and tolerability of oral treatment with living bacteria of E. coli DSM 17252 (Symbioflor®2) in pati... | ||
Medical condition: Diarrhoea-predominant irritable bowel syndrome with recurrent abdominal pain according to Rome IV criteria | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002313-18 | Sponsor Protocol Number: PAMORA-AP_2020 | Start Date*: 2020-12-22 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: The effects of opioid receptor antagonism on acute pancreatitis: An investigator initiated, randomized, placebo-controlled, double-blind clinical trial | |||||||||||||
Medical condition: Acute pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005528-13 | Sponsor Protocol Number: 30112012 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Helsinki University Hospital | |||||||||||||
Full Title: Comparison of Novel Articaine Lozenge Versus Placebo for Upper Gastrointestinal Endoscopy in Adults. A Randomized Double-blinded Controlled Study | |||||||||||||
Medical condition: Patients who undergo esophagogastroduodenoscopy procedure for a first time | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000533-31 | Sponsor Protocol Number: 17GA001 | Start Date*: 2017-11-07 | ||||||||||||||||
Sponsor Name:Nottingham University Hospitals NHS Trust | ||||||||||||||||||
Full Title: TReatment of Irritable bowel syndrome using Titrated ONdansetron Trial | ||||||||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhoea | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001776-19 | Sponsor Protocol Number: 2010-19 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bombastus-Werke AG | |||||||||||||
Full Title: MULTICENTRIC RANDOMIZED PLACEBO-CONTROLLED DOUBLE-BLIND 2-ARM PIVOTAL STUDY ON EFFICACY AND SAFETY OF ARHAMA®-TINKTUR N IN PATIENS WITH ACUTE DIARRHEA | |||||||||||||
Medical condition: Acute unspecific diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002613-10 | Sponsor Protocol Number: STW5/212-D-011-III-V | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Steigerwald Arzneimittelwerk GmbH | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled study on the efficacy of Iberogast® (STW 5) in patients with irritable bowel syndrome | |||||||||||||
Medical condition: Irritable Bowel Syndrome (IBS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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