- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
9 result(s) found for: Peppermint.
Displaying page 1 of 1.
| 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: 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: 2008-006413-25 | Sponsor Protocol Number: GA0821 | Start Date*: 2008-12-09 |
| Sponsor Name:Reckitt Benckiser Healthcare (UK) Limited | ||
| Full Title: A single-centre randomised, partially blind, single dose, crossover study investigating the onset of action of soothing and cooling after taking Gaviscon Peppermint liquid, Double Action Gaviscon ... | ||
| Medical condition: Symptoms of heartburn | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-021630-63 | Sponsor Protocol Number: GA1001 | Start Date*: 2011-03-28 |
| Sponsor Name:Reckitt Benckiser | ||
| Full Title: A randomised, double blind placebo controlled study in patients with reflux symptoms to assess suppression of gastro-oesophageal reflux by ‘Gaviscon Double Action Peppermint liquid’ using the BRAVO... | ||
| Medical condition: Gastro-oesophageal reflux disease (GORD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-019072-68 | Sponsor Protocol Number: version 1 (07/10/2010) | Start Date*: 2010-12-31 |
| Sponsor Name:Guy's & St Thomas' NHS Foundation Trust | ||
| Full Title: A randomised, double blind, crossover study to determine the mechanism of action of Gaviscon Advance in Gastro-Oesophageal Reflux Disease (GORD) | ||
| Medical condition: Gastro-oesophageal reflux disease (GORD) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003976-38 | Sponsor Protocol Number: IBO | Start Date*: 2020-04-23 | ||||||||||||||||
| Sponsor Name:Fundació Institut d’Investigació en Ciències de la Salut Germans Trias i Pujol (IGTP) | ||||||||||||||||||
| Full Title: EFFECT OF STW5 (Iberogast ®) AND STW5-II (Iberogast N®) ON TRANSIT AND TOLERANCE OF INTESTINAL GAS | ||||||||||||||||||
| Medical condition: Irritable bowel syndrome and functional dyspepsia | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-004777-89 | Sponsor Protocol Number: CAS/B/016611 | Start Date*: 2012-02-28 | |||||||||||
| Sponsor Name:Cassella-med GmbH & Co. KG | |||||||||||||
| Full Title: Efficacy and safety of Euminz® (10% ethanolic solution of peppermint oil for topical use) compared to placebo in patients with episodic tension-type headache (ETTH) | |||||||||||||
| Medical condition: Episodic tension-type headache | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005821-31 | Sponsor Protocol Number: GA0706 | Start Date*: 2008-01-15 |
| Sponsor Name:Reckitt Benckiser Healthcare UK) Limited [...] | ||
| Full Title: A single-centre randomised, partially blind, single dose, crossover pilot study investigating the use of stopwatches to assess the onset of action of soothing and cooling of Gaviscon Peppermint Liq... | ||
| Medical condition: Symptoms of heartburn | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022082-10 | Sponsor Protocol Number: ZEG/01-2010 (GERD) | Start Date*: 2011-02-09 |
| Sponsor Name:Norgine Ltd | ||
| Full Title: A double-blind, double-dummy, randomised, study to assess the superiority of Zegerid® 20 mg vs. Losec® 20 mg in the rapid relief of heartburn associated with GERD as on demand therapy. | ||
| Medical condition: Heartburn associated with gastro-oesophageal reflux disease (GERD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) CZ (Completed) HU (Completed) BG (Completed) | ||
| Trial results: View results | ||
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