Evaluation of Locally Delivered Propolis Gels in Periodontitis

NAActive, not recruitingINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

September 17, 2023

Primary Completion Date

June 24, 2024

Study Completion Date

December 31, 2024

Conditions
Periodontal Diseases
Interventions
DRUG

Study Group

"It will include 16 patients with periodontitis stage II, grade B, at least 2 sites with pocket PD = 4-5 mm and CAL = 3-4 mm each will receive non-surgical periodontal therapy followed by application of propolis gel.~After baseline assessment, at the same day the included participants will receive full mouth one stage debridement using hand instruments and ultrasonic scalers under local anesthesia -if needed- for patient's comfort.~2- Oral Hygiene Instructions Participants will be provided with a toothpaste, a medium toothbrush, a written oral hygiene instruction brochure (Brushing twice daily for 4-weeks using Modified Bass technique and interdental flossing).~3-Base line visit (Local delivery application): Propolis gel will be applied by syringe with blunt tip gently and removed slowly in order not to harm the tissue for group 1 patients (Test group) after phase 1 therapy at the second day (48 hours) following non-surgical periodontal therapy"

DRUG

Control (placebo) group

"After baseline assessment, at the same day the included participants will receive full mouth one stage debridement using hand instruments and ultrasonic scalers under local anesthesia -if needed- for patient's comfort.~2- Oral Hygiene Instructions Participants will be provided with a toothpaste, a medium toothbrush, a written oral hygiene instruction brochure (Brushing twice daily for 4-weeks using Modified Bass technique and interdental flossing)."

Trial Locations (1)

4393005

faculty of dentistry Ain Shams University, Cairo

All Listed Sponsors
lead

Ain Shams University

OTHER

NCT06663995 - Evaluation of Locally Delivered Propolis Gels in Periodontitis | Biotech Hunter | Biotech Hunter