NCT07426198Completed
The Effect of Oral Care With Propolis in COPD Patients
THE EFFECT OF ORAL CARE WITH PROPOLIS ON THE DEVELOPMENT OF ORAL MUCOSITIS IN PATIENTS WITH CHRONIC OBSTRUCTIVE PULMONARY DISEASE RECEIVING TREATMENT IN THE INTENSIVE CARE: A RANDOMIZED CONTROLLED TRIAL
Source: ClinicalTrials.gov · Last updated 23 Feb 2026
Brief summary (registry, in English)
The study was conducted in intensive care units and included patients diagnosed with COPD. The study was conducted with a total of 60 COPD patients, 30 in the intervention group and 30 in the control group. Individuals in the intervention group were given an oral care protocol containing propolis for 15 days, in addition to the clinic's standard oral care protocol. The control group continued to receive standard oral care. Oral mucosa was assessed on days 1, 7 and 15.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 16 Feb 2026
- Start date
- 1 Jan 2025
- Primary completion date
- 10 Jun 2025
- Lead sponsor
- TC Erciyes University
- Diseases
- COPD
- NCT number
- NCT07426198
What you commit to
- Study type: Interventional
- Participants enrolled: 60
- From 1 Jan 2025 to the primary completion date, 10 Jun 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- individuals receiving immunosuppressive therapy,
- individuals receiving mechanical ventilation support,
Other illness
- individuals with a cancer diagnosis,
Other
- individuals with altered consciousness or acute confusion,
- individuals who did not volunteer to participate in the study were excluded from the research.
Who the study is looking for
- Aged 18 years or older,
- diagnosed with COPD,
- no oral mucositis at the start of the study,
- no known allergy to bees or bee products,
- able to speak and understand Turkish and communicate effectively,
- conscious,
- without any psychiatric illness,
- without any mental or physical disability that would prevent them from answering questions,
- individuals who volunteered to participate in the study were included in the study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Erciyes University Coordinator of this site? Confirm its status | Talas | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.