The Effects of an Aromatic Botanical Extract on Respiratory Health.
Not Applicable
Completed
- Conditions
- Respiratory Health
- Interventions
- Dietary Supplement: Teramune Botanical ExtractOther: Placebo
- Registration Number
- NCT04368169
- Lead Sponsor
- Franklin Health Research
- Brief Summary
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.
- Detailed Description
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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 71
Inclusion Criteria
- age: 18-60 years
- currently experiencing respiratory symptoms
- otherwise healthy
Exclusion Criteria
- underlying respiratory conditions
- pregnant, breastfeeding, or trying to conceive
- tobacco use in the home
- allergies to any of the ingredients
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Aromatic Extract Teramune Botanical Extract Participants receive the aromatic botanical extract orally every 4-6 waking hours for 3 days. Placebo Placebo Participants receive the placebo matching the botanical extract orally every 4-6 waking hours for 3 days.
- Primary Outcome Measures
Name Time Method Change from baseline on the 44-part Wisconsin Upper Respiratory Symptom Survey (WURSS-44) at day 3. Baseline and 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.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Franklin School of Integrative Health Sciences
🇺🇸Franklin, Tennessee, United States