HALEON
This study is designed to generate real world data from participants with nasal congestion acquired from common cold following treatment with a marketed nasal spray. The main purpose of this study is to evaluate the effectiveness of a nasal spray on quality of life (QoL) factors.
Common Cold
Otrivine Congestion Relief
Phase 4
This is a longitudinal, open-label study evaluating the effect on QoL factors in participants with the common cold using Otrivine nasal spray (xylometazoline hydrochloride 0.1 percent [%]), in a real-world setting. A sufficient number of adults aged 18 years and over with symptoms of common cold will be screened for eligibility. The study expects to enroll approximately 125 participants to ensure that 100 participants complete the study. All study data will be collected remotely through a study app using the participant's own mobile device.}}
Study Type : | Interventional |
Estimated Enrollment : | 136 participants |
Masking : | None (Open Label) |
Primary Purpose : | Treatment |
Official Title : | A Real-World Evidence Study Evaluating Quality of Life Parameters Following Treatment With Otrivine (Xylometazoline Hydrochloride) |
Actual Study Start Date : | November 7, 2022 |
Estimated Primary Completion Date : | December 20, 2022 |
Estimated Study Completion Date : | December 20, 2022 |
Arm | Intervention/treatment |
---|---|
Experimental: Otrivine Congestion Relief Participants will be instructed to use the product per label and leaflet instructions: 1 spray in each nostril up to 3 times per day until resolution of symptoms or up to a maximum of 7 days, whichever occurs first. |
Drug: Otrivine Congestion Relief |
Ages Eligible for Study: | 18 Years |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
Not yet recruiting
The VCTC
Swadlincote, Derbyshire, United Kingdom, DE11 7AQ