Trials / Completed
CompletedNCT07460934
Effect of Pleuran on the Clinical Course of Patients With Chronic Rhinosinusitis
Effect of Pleuran on the Clinical Course of Patients With Chronic Rhinosinusitis - EPCCOR Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 85 (actual)
- Sponsor
- Pleuran, s.r.o. · Industry
- Sex
- All
- Age
- 12 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical research is to learn if Imunoglukan P4H® as an add-on therapy to the standard of care treatment according to the EPOS guidelines (intranasal corticosteroids and saline irrigation) can help to prevent CRS exacerbations, respiratory tract infections and reduce the use of antibiotics and intranasal corticosteroids in newly diagnosed children over 12 years of age and adults with CRS without nasal polyps. The investigational product, Imunoglukan P4H® capsules, will be added to the standard of care treatment according to the EPOS guidelines (intranasal corticosteroids and saline irrigation) as prescribed by their treating physician.
Detailed description
Participants: Newly diagnosed patients over 12 years of age with a diagnosis of chronic rhinosinusitis without nasal polyps meeting the inclusion criteria. Sites: 5; Czech republic (2) and Slovakia (3) Study duration: 12 moths: 3 months treatment + 3 months follow-up + 3 months treatment + 3 months follow-up Randomization: * Control group: Standard of care treatment according to EPOS guidelines (INCS and saline irrigation) * Active group: Standard of care treatment according to EPOS guidelines (INCS and saline irrigation) + Imunoglukan P4H® capsules (IMG® 100 mg + Vitamin C 100 mg in 1 capsule) Participants will: * take standard of care treatment according to EPOS guidelines. * take Imunoglukan P4H® every day for 3 months then there will be three months follow-up (without Imunoglukan P4H®), this cycle will be repeated twice (only participants in the active group). * visit the clinic for control visits one month after the study initiation and then every three months during 12 months study period (SNOT-22 questionnaire, VAS scale for evaluation of CRS severity by treating physician, Swab from the upper aerodigestive tract, rhinoendoscopic examination) * keep a diary of their symptoms (incidence and duration of CRS exacerbations and acute respiratory infections, use of antibiotics, use of intranasal corticosteroids and other symptomatic treatments) * record number of emergency department visits, hospitalizations, doctor visits and missed work/school days. * record incidence of potential adverse events
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Imunoglukan P4H® capsules | 1 capsule contains 100 mg of IMG® and 100 mg of vitamin C |
Timeline
- Start date
- 2022-11-01
- Primary completion
- 2025-12-31
- Completion
- 2025-12-31
- First posted
- 2026-03-10
- Last updated
- 2026-03-10
Locations
5 sites across 2 countries: Czechia, Slovakia
Source: ClinicalTrials.gov record NCT07460934. Inclusion in this directory is not an endorsement.