Table of contents
- Trial overview
- Study design and phase
- Who can participate
- What is being measured
- Why this study matters
Trial overview
The clinical trial with NCT ID 2025-520845-61-00 is studying LIQUID EXTRACT OF THYME (1:3.45-3.85), EXTRACTION SOLVENT: ETHANOL 27%(V/V) in children with acute bronchitis.[1] The study is designed to assess whether the treatment can help in this condition and whether it is safe to use in the target group.[1]
Study design and phase
This is an interventional study, which means the researchers give a treatment and then measure the results.[1] It is described as double-blind, randomized, and placebo-controlled.[1] These terms mean that treatment groups are assigned by chance, and neither the participants nor the researchers know who receives the study treatment or the placebo during the trial.[1] The trial is listed as Phase 3 and has an enrollment of 56 participants.[1]
Who can participate
The target population is pediatric patients, meaning children.[1] The trial data do not provide more detailed age limits or other eligibility rules.[1] The study focuses on children who have acute bronchitis.[1]
What is being measured
The main endpoint is the efficacy of the investigational product based on the Bronchitis Severity Score.[1] Efficacy means how well the treatment works in the study.[1] The Bronchitis Severity Score is used to measure how severe the bronchitis symptoms are.[1]
The brief summary also says the study is looking at safety and at whether the treatment may help reduce inappropriate antibiotic use in acute bronchitis in children.[1] This shows that the trial is not only about symptom relief, but also about better treatment use in practice.[1]
Why this study matters
Acute bronchitis in children can lead to treatment decisions that are not always ideal, including antibiotic use when it may not be needed.[1] This trial is trying to learn whether LIQUID EXTRACT OF THYME (1:3.45-3.85), EXTRACTION SOLVENT: ETHANOL 27%(V/V) can be a useful option for this condition in a controlled research setting.[1] Because the study is placebo-controlled, it can help compare the study treatment with a look-alike treatment that has no active drug.[1]
Trial details at a glance
| Item | Information |
|---|---|
| Trial ID | 2025-520845-61-00 |
| Status | Authorised |
| Condition | Acute bronchitis |
| Population | Pediatric patients |
| Design | Double-blind, randomized, placebo-controlled |
| Phase | Phase 3 |
| Enrollment | 56 |
| Main endpoint | Efficacy based on the Bronchitis Severity Score |



