The Effect of Oral Care With Propolis in COPD Patients

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.

NCT Number	NCT07426198
Lead Sponsor	TC Erciyes University
Conditions	Oral Mucositis
Enrollment	60 participants
Start Date	2025-01-01
Primary Completion	2025-06-10 (estimated)
Study Completion	2025-06-10 (estimated)
Updated on ClinicalTrials.gov	2026-02-23