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| ID | Type | Description | Link |
|---|---|---|---|
| Rakover1 |
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This randomized, double blind, parallel group study, compared the efficacy of spray containing aromatic essential oils of some herbal plants, against placebo in the treatment of patients with acute viral Pharyngo-tonsillitis.
Study objectives: Primary to demonstrate a throat pain relief within 20 minutes after first administration of treatment with the spray.
Secondary to demonstrate a reduction of a defined symptoms sum score based on symptoms and signs comparing baseline therapy from the beginning to the end of 3 days treatment
This study compared the efficacy of spray containing aromatic essential oils of Eucalyptus citriodora, Eucalyptus globulus, Mentha piperita, Origanum syriacum, and Rosmarinus Officinalis, against placebo in the treatment of patients with acute viral Pharyngo-tonsillitis.
In- vitro and clinical studies suggest therapeutic potential of aromatic herbs and trees oils in the treatment of Pharyngo-Tonsillitis. The pharmacological and clinical activity of Eucalyptus citriodora, Eucalyptus globulus, Mentha piperita, Origanum syriacum, and Rosmarinus Officinalis, include anti-inflammatory, anti-bacterial and anti-viral activities. Some of these herbs and trees oils have direct activity on the respiratory tract, the coughing reflex and the airflow in the nasal tract.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Active Comparator | treatment with spray containing aromatic essential oils of some herbal plants. |
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| 2 | Placebo Comparator | spray containing placebo. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| mixture of aromatic essential oils. | Dietary Supplement | 3% of mixture containing aromatic essential oils of Eucalyptus citriodora, Eucalyptus globulus, Mentha piperita, Origanum syriacum, and Rosmarinus Officinalis, spraying to the throat. |
| Measure | Description | Time Frame |
|---|---|---|
| To demonstrate a throat pain relief within the first 20 minutes after first administration of treatment with the spray. | 20 minutes |
| Measure | Description | Time Frame |
|---|---|---|
| To demonstrate a reduction of a defined symptoms sum score based on symptoms and signs comparing baseline therapy from the beginning to the end of 3 days treatment. | 3 days |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Yoseph Rakover, M.D. | haemek medical center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Otorhinolaryngology department | Afula | 18101 | Israel |
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| placebo | Dietary Supplement | 0:1% of Lemon VIP (Florasynth,Israel), spraying to the throat. |
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