WHO ICTRP trial
A single-centre randomised, partially blind, single dose, crossover study…
EUCTR2008-006413-25-GB · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2008-006413-25-GB |
|---|---|
| Public 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 liquid, Gaviscon Instants Oral Powder, compared to a control in subjects with heartburn following a refluxogenic meal, using the 2-stopwatch technique - Gaviscon Soothing and Cooling |
| Scientific 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 liquid, Gaviscon Instants Oral Powder, compared to a control in subjects with heartburn following a… |
| Primary sponsor | Reckitt Benckiser Healthcare (UK) Limited |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Countries | United Kingdom |
| Conditions | Symptoms of heartburn |
| Interventions | Trade Name: Gaviscon Peppermint Liquid Relief Product Name: Gaviscon Peppermint Liquid Relief Pharmaceutical Form: Oral suspension CAS Number: 9005383 Other descriptive name: SODIUM ALGINATE Concentration unit: mg milligram(s) Concentration… |
| Registration date | Jan 19, 2009 |
| Secondary IDs | GA0821 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: