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The Effects of an Aromatic Botanical Extract on Respiratory Health.

F

Franklin Health Research

Status

Completed

Conditions

Respiratory Health

Treatments

Dietary Supplement: Teramune Botanical Extract
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT04368169
20-4-9100

Details and patient eligibility

About

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.

Full 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.

Enrollment

71 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

71 participants in 2 patient groups, including a placebo group

Aromatic Extract
Experimental group
Description:
Participants receive the aromatic botanical extract orally every 4-6 waking hours for 3 days.
Treatment:
Dietary Supplement: Teramune Botanical Extract
Placebo
Placebo Comparator group
Description:
Participants receive the placebo matching the botanical extract orally every 4-6 waking hours for 3 days.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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