Clinical Trials Directory

Trials / Completed

CompletedNCT02100605

Study on Hypertonic Saline Nasal Spray

A Study to Assess the Speed of Relief From Nasal Congestion With a Hypertonic Saline Nasal Spray (Phytosun Decongestant)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Omega Pharma · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Phytosun decongestant nasal spray is a class I medical device registered in the European Union for the treatment of nasal congestion. The spray contains hypertonic seawater and essential oils. The objective of the study is to investigate the effects of a nasal spray, registered as a medical device under the name Phytosun Decongestant in the European Union, on speed of onset of relief of nasal congestion in 50 subjects suffering from nasal congestion associated with common cold.

Detailed description

The study will also include an exploratory assessement of any objective changes in nasal patency by measuring nasal peak inspiratory flow before and after treatment.

Conditions

Interventions

TypeNameDescription
DEVICEPhytosun, decongestant, nasal sprayone time application of the nasal spray

Timeline

Start date
2014-03-01
Primary completion
2014-10-01
Completion
2014-10-01
First posted
2014-04-01
Last updated
2015-02-20

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02100605. Inclusion in this directory is not an endorsement.