- Trials with a EudraCT protocol (65)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
65 result(s) found for: Common cold.
Displaying page 1 of 4.
EudraCT Number: 2013-002785-39 | Sponsor Protocol Number: BRN-C-2013-04 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Laboratoires BOIRON | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004524-11 | Sponsor Protocol Number: 2013105 | Start Date*: 2013-12-16 | ||||||||||||||||
Sponsor Name:Proctor and Gamble Technical Centres Ltd | ||||||||||||||||||
Full Title: A 2-arm, randomised, single - (investigator) blind, controlled, parallel design study in common cold sufferers experiencing cough and nasal congestion to assess the effects of Vicks® VapoRub® (VVR)... | ||||||||||||||||||
Medical condition: Sleep disruption due to cough and nasal congestion during a cold. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004641-34 | Sponsor Protocol Number: RM-0205 | Start Date*: 2006-02-07 |
Sponsor Name:Matrixx Initiatives Inc | ||
Full Title: Human Clinical Study: Assessment of Zicam Cold Remedy RapidMelts | ||
Medical condition: to shorten the duration, reduce the number and decrease the sevity of common cold symptoms in otherwise healthy human adult volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022441-21 | Sponsor Protocol Number: 701004.01.012 | Start Date*: 2010-12-13 | |||||||||||
Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
Full Title: EPs® 7630 film-coated tablets in subjects (≥18 years old) suffering from common cold A prospective, multi-center, single-arm, open-label, phase IV clinical post-marketing safety study | |||||||||||||
Medical condition: Common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022857-41 | Sponsor Protocol Number: C6930943 | Start Date*: 2010-12-14 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: Effects of a common cold treatment on cognitive function | |||||||||||||
Medical condition: Common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004977-28 | Sponsor Protocol Number: 701079.01.013 | Start Date*: 2014-02-06 | |||||||||||
Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
Full Title: Safety and intake effect of EPs®7630 (an extract from the roots of Pelargonium sidoides) | |||||||||||||
Medical condition: common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000860-51 | Sponsor Protocol Number: CASK0120 | Start Date*: 2020-06-25 | |||||||||||
Sponsor Name:Cassella-med GmbH & Co. KG | |||||||||||||
Full Title: The effect of early administered cineole on the course of a common cold | |||||||||||||
Medical condition: common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002058-96 | Sponsor Protocol Number: SAN-0657 | Start Date*: 2021-11-16 | ||||||||||||||||
Sponsor Name:Lek Pharmaceuticals d.d. | ||||||||||||||||||
Full Title: Efficacy and safety of the combination of acetylcysteine, paracetamol and phenylephrine for the treatment of common cold: a prospective, randomized, double-blind, controlled trial | ||||||||||||||||||
Medical condition: Common cold and flu-like infections | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Prematurely Ended) PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004466-14 | Sponsor Protocol Number: RH01361 | Start Date*: 2011-10-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: Effects of two doses of a common cold treatment on cognitive function | |||||||||||||
Medical condition: Common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021798-34 | Sponsor Protocol Number: C7100991 | Start Date*: 2010-09-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare (GSKCH) | |||||||||||||
Full Title: To assess the subjective effect of two paracetamol preparations on the feeling of breathing in subjects with the common cold. | |||||||||||||
Medical condition: Common cold and flu | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005797-31 | Sponsor Protocol Number: 701004.01.007 | Start Date*: 2008-08-14 | |||||||||||
Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
Full Title: Efficacy and tolerability of EPs® 7630 film-coated tablets in patients (>=18 years old) with Acute Rhinopharyngitis (ARP) | |||||||||||||
Medical condition: Adult patients suffering from Acute Rhinopharyngitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000057-31 | Sponsor Protocol Number: ESTUAR001 | Start Date*: 2012-03-19 | ||||||||||||||||||||||||||
Sponsor Name:THERANOR sprl | ||||||||||||||||||||||||||||
Full Title: Multicentre, randomised, double-blind, parallel, placebo-controlled study evaluating the efficacy and safety of Early Self-Treatment of viral Upper respiratory tract infections with homeopathic ora... | ||||||||||||||||||||||||||||
Medical condition: Viral upper respiratory tract infections | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006690-25 | Sponsor Protocol Number: OTCS-CE-301 | Start Date*: 2007-02-09 | |||||||||||
Sponsor Name:Novartis Consumer Health SA | |||||||||||||
Full Title: A Double-Blind, Randomized, Parallel Group, Placebo Controlled Study, Evaluating the Decongestant Effect, Time to Onset, Duration of Effect and Impact on Sleep and General Well-being of Otrivin F2 ... | |||||||||||||
Medical condition: nasal congestion associated with the common cold | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005442-23 | Sponsor Protocol Number: 411-LY-08-01-0000 | Start Date*: 2009-02-19 | ||||||||||||||||
Sponsor Name:Leyh Pharma GmbH | ||||||||||||||||||
Full Title: Evaluation of the efficacy and safety of nose spray containing 3% silver protein diacetyl tannate (SEAT) in patients with uncomplicated viral rhinitis. A placebo-controlled, randomized, multicentri... | ||||||||||||||||||
Medical condition: treatment of uncomplicated rhinal infections | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003559-32 | Sponsor Protocol Number: CPO19001 | Start Date*: 2023-03-16 | ||||||||||||||||
Sponsor Name:PharOS Pharmaceutical Oriented Services Single Member Ltd. | ||||||||||||||||||
Full Title: A Phase III Prospective, Randomized, Multicenter, Double-Blind, Placebo-controlled clinical study to evaluate the efficacy and safety of fixed dose combination (FDC) product Ibuprofen/Paracetamol/P... | ||||||||||||||||||
Medical condition: Temporary relief of cold and flu symptoms, i.e. mild to moderate pain, sore throat, fever and nasal congestion | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001637-41 | Sponsor Protocol Number: A7801001 | Start Date*: 2005-07-26 |
Sponsor Name:Pfizer Consumer Healthcare cva/sca | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® (Paracetamol (500mg)/Pseudoephedrine (30mg)) on subjects with nasal congestion accompanied by h... | ||
Medical condition: Medical rationale= Investigation of combination drug Sinutab in symptomatic relief of common cold with nasal symptoms. Community pharmacists are considered as local investigators including subjec... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000058-35 | Sponsor Protocol Number: A7801002 | Start Date*: 2006-04-26 |
Sponsor Name:Pfizer Consumer Healthcare Comm. VA/SCA | ||
Full Title: A community pharmacy based investigation in the self-medication area Efficacy and safety of Sinutab® [Paracetamol (500mg) and Pseudoephedrine (30mg)] on subjects with nasal congestion accompanied ... | ||
Medical condition: The medical rationale = to investigate this combination drug in the symptomatic relief of common cold with nasal symptoms. The reduction of symptom severity may allow subjects receiving active medi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012640-17 | Sponsor Protocol Number: KJos/FIN | Start Date*: 2009-12-10 |
Sponsor Name:Swedish Herbal Institute | ||
Full Title: A randomized, controlled, parallel-group, double-blind study of the proprietary Kan Jang Oral Solution versus placebo in patients with non complicated respiratory tract infections (common cold). | ||
Medical condition: common cold | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012297-12 | Sponsor Protocol Number: 920134 | Start Date*: 2009-08-12 |
Sponsor Name:Bioforce AG | ||
Full Title: Safety and Efficacy of long-term treatment with Echinaforce® over 4 months | ||
Medical condition: common cold | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2013-005006-66 | Sponsor Protocol Number: 2013118 | Start Date*: 2014-01-21 |
Sponsor Name:Procter and Gamble | ||
Full Title: A 2-arm, randomised, single - (Investigator) blind, controlled, parallel design study in common cold sufferers experiencing nasal congestion to assess the speed of action of Vicks® VapoRub® (VVR) | ||
Medical condition: Nasal congestion due to common cold in adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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