The Effects of an Aromatic Botanical Extract on Respiratory Health.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Respiratory Health

See also
Status	Clinical Trial	Phase
Not yet recruiting	`NCT04170881` - CRESPI - Respiratory Health of Children in Daycare
Recruiting	`NCT04758845` - Clinical Study to Evaluate the Safety and Efficacy of New Probiotic Strains in Health Adults	N/A
Recruiting	`NCT04812561` - Effects of Bronch™ on Respiratory Health	N/A

See also

Status

Clinical Trial

Phase

Not yet recruiting

NCT04170881 - CRESPI - Respiratory Health of Children in Daycare

Recruiting

NCT04758845 - Clinical Study to Evaluate the Safety and Efficacy of New Probiotic Strains in Health Adults

N/A

Recruiting

NCT04812561 - Effects of Bronch™ on Respiratory Health

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT04368169
Study type	Interventional
Source	Franklin School of Integrative Health Sciences
Contact
Status	Completed
Phase	N/A
Start date	April 27, 2020
Completion date	November 30, 2020

The Effects of an Aromatic Botanical Extract on Respiratory Health.

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms