Functional Honey for Sore Throat Relief
Honey
Infections+4
+ Stomatognathic Diseases
+ Otorhinolaryngologic Diseases
Treatment Study
Summary
Study start date: January 6, 2022
Actual date on which the first participant was enrolled.This study focuses on finding out how different types of honey can help people with sore throats feel better. It involves patients who are already receiving standard treatment for sore throat. The researchers are testing five kinds of honey, each with unique properties like high antioxidant or antimicrobial activities, to see if they can provide additional relief from symptoms. This study is important because it could offer a natural and easily accessible way to relieve sore throat symptoms, which can be common and uncomfortable. During the study, participants are asked to take 15 grams of their assigned type of honey twice a day for ten days. They are observed and checked on the 1st, 3rd, 7th, and 10th days to see how their symptoms change, including sore throat severity, difficulty swallowing, and feelings of fatigue. This process helps researchers understand if and how the honey is helping to reduce these symptoms. The study does not mention any specific risks, but the potential benefit is finding a new way to ease sore throat discomfort.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.282 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: Adults presenting with sore throat symptoms due to an upper respiratory infection (URI) within the last four days were included in the study. A total of 300 patients over 18 years of age, who were prescribed necessary medication and exhibited signs and symptoms of sore throat, were enrolled. Exclusion Criteria: Exclusion criteria included a history of diabetes, pollen or bee allergies, and aversion to honey. Participants were required not to use any additional products outside of those provided by the researchers during the study period. Written informed consent was obtained from all participants, who were then randomly assigned to either the study or control group.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.6 intervention groups are designated in this study
16.667% chance of being blinded to the placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorGroup III
Active ComparatorGroup IV
Active ComparatorGroup 5
Active ComparatorGroup 6
PlaceboStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Istanbul Medipol University
Istanbul, Turkey (Türkiye)Open Istanbul Medipol University in Google Maps