Evaluation of iPRF With Vitamin C in StageII Grade A Periodontitis

Periodontitis Clinical Trial

Official title:

Evaluation of Injectable PRF With Vitamin C as an Adjunct to Non-surgical Therapy in the Treatment of Stage II Grade A Periodontitis. A Randomized Controlled Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05129267
• Other study ID #: PER 3- 3- 2
• Status: Recruiting
• Phase: N/A
• Start date: October 3, 2021
• Est. completion date: June 2, 2022

Study information

• Verified date: November 2021
• Source: Cairo University
• Contact: Mohamed Ab Sherif
• Phone: 01118222827
• Email: mohamedsherif[@]dentistry.cu.edu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Comparing the effect of using vitamin C with injectable PRF as a locally delivered adjunct to scaling and root planing versus scaling and root planing with local delivery of injectable PRF and scaling and root planing alone on the clinical parameters in Stage II Grade A Periodontitis patients.

Description:

The conventional approach: Group 1: Scaling and root planing alone using Gracey curettes and ultrasonic scalers. Group 2: Scaling and root planing using Gracey curettes and ultrasonic scalers with local delivery of injectable PRF using an insulin syringe with the blunt needle inserted into the bottom of the periodontal pocket through a template to hold the locally delivered injectable PRF. The intervention approach: Scaling and root planing using Gracey curettes and ultrasonic scalers with local delivery of vitamin C (250 μM) and injectable PRF, using an insulin syringe with the blunt needle inserted into the bottom of the periodontal pocket through a template to hold the locally delivered vitamin C and injectable PRF for a longer time.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 45
• Est. completion date: June 2, 2022
• Est. primary completion date: June 2, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients with healthy systemic condition.

2. Adult patients ? 18 years old.

3. Patients with Stage II Grade A periodontitis.

4. Patients accept 6-months follow-up period (cooperative patients).

5. Patients provide an informed consent.

Exclusion Criteria:

1. Presence of prosthetic crowns.

2. Extensive restorations.

3. Periodontal therapy within the last 12 months.

4. Having surgical therapy or undergoing orthodontic treatment.

5. Ongoing drug therapy that might have an impact on the clinical signs and symptoms of periodontitis.

6. The use of antibiotics or anti-inflammatory drugs 1 month prior to the procedure and till the end of 6 months of follow-up.

7. Smokers.

8. Pregnant females.

Related Conditions & MeSH terms

• Periodontitis

Intervention

Other:
• Group B
Scaling and Root debridement + iPRF
• Group C
Scaling and Root debridement + iPRF together with vitamin C

Locations

Country	Name	City	State
Egypt	Faculty of Oral and Dental Medecine-CU	Cairo

Sponsors (1)

Lead Sponsor	Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Bleeding on Probing (BOP)	Gentle probing of the orifice of the gingival crevice. The periodontal probe will be inserted 1 to 2 mm into the gingival sulcus starting at one interproximal area and moving to the other. If bleeding occurs within 10 seconds a positive finding is recorded.	3 months
Secondary	Probing Depth (PD)	Measured from the gingival margin to the bottom of the gingival sulcus. Each tooth will be probed with a light force not exceeding 25 grams at 6 sites.	6 months
Secondary	Clinical Attachment Level (CAL)	Measured from the CEJ to the bottom of the gingival sulcus, or will be calculated as the algebraic sum of gingival recession and PD measurements for each site. Each tooth will be probed with a light force not exceeding 25 grams at six points: (mesio-buccal, mid-buccal, disto-buccal, mesio-lingual, mid-lingual, and disto-lingual).	6 months
Secondary	Gingival Marginal Level (GML)	Measured from the free gingiva to CEJ.	6 months
Secondary	Plaque Index (PI)	Teeth in each quadrant will be dried with a blast of air, and presence of visible dental plaque will be recorded with scores 0, 1, 2, 3.	6 months
Secondary	Intraoral Radiographs	A customized X-ray positioning stent will be fabricated to allow easy and accurate radiographing and retain the plastic film holder in the paralleling radiographic technique.	6 months
Secondary	Post-Operative Pain	Visual Analogue Scale (VAS) with numbers from 0 to 10 ('no pain' to 'worst pain imaginable') measured daily for the first 2 days postoperatively.	48 hours