Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This study is a randomized, double blind, placebo controlled, intervention study evaluating the effect of an aromatic botanical extract on overall respiratory health among otherwise healthy adults.
After being informed about the study and providing informed consent, patients with respiratory complaints will be randomized into a double blind placebo controlled trial of the botanical extract.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Aromatic Extract | Experimental | Participants receive the aromatic botanical extract orally every 4-6 waking hours for 3 days. |
|
| Placebo | Placebo Comparator | Participants receive the placebo matching the botanical extract orally every 4-6 waking hours for 3 days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Teramune Botanical Extract | Dietary Supplement | Combination blend of aromatic plant extracts in an emulsifier carrier. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline on the 44-part Wisconsin Upper Respiratory Symptom Survey (WURSS-44) at day 3. | The Wisconsin Upper Respiratory Symptom Survey (WURSS-44) is a validated, self reported instrument assessing overall respiratory health. Possible scores range from 0 to 308 with lower scores indicating fewer respiratory complaints. | Baseline and Day 3 |
Not provided
Not provided
Inclusion Criteria:
Exclusion Criteria:
self identify as female
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Jessie H Hawkins, PhD | Nutraceuticals Research Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Franklin School of Integrative Health Sciences | Franklin | Tennessee | 37067 | United States |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Participants are recruited through a single health practice and randomized through block randomization to one of 2 groups: botanical extract or inert control.
Not provided
Not provided
Double Blind
| Placebo | Other | Emulsifier carrier without active supplement ingredients. |
|