Actively Recruiting
3-Month Clinical Trial of Liquid S-PRF in Periodontal Debridement for Periodontitis Stages II-IV
Led by Mahsa University · Updated on 2025-12-19
14
Participants Needed
1
Research Sites
99 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
What is the purpose of this study? This study is to investigate the effect of a processed blood product in healing after treatment for gum disease. In addition to scaling \& root debridement (deep cleaning) that is the standard treatment for periodontitis, this study will test the effectiveness of patient's processed blood in improving healing of diseased gums. What are the procedures to be followed? First, all patients will undergo dental check-up and X-ray imaging for suitability as a participant for the project. For participants who are eligible and included into study, upper \& lower jaws models will be made, and each will be given oral care kit \& instructions. The next appointment will be given for scaling \& root debridement with local numbing agent in one day. Towards the end of the treatment, a small amount (20 mℓ) of blood will be collected and spun to produce liquid platelet-rich fibrin that is then used to flush the treated gum pockets in half of the mouth. For the treated gum pockets in the opposite half of the mouth, sterile salt water (saline) will be used instead for comparison. Then, follow-up appointments are at monthly intervals until 3 months. Who should enter the study? Symptoms of gum disease include bleeding and/or receding gums, tooth/teeth appearing longer or feeling shaky/loose/weak, formation of large amount of calculus and/or black/empty space between teeth, frequent/recurrent gum swelling/pus, and/or bad breath.
CONDITIONS
Official Title
3-Month Clinical Trial of Liquid S-PRF in Periodontal Debridement for Periodontitis Stages II-IV
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Have at least 20 teeth
- American Society of Anesthesiology class I or II
- Diagnosed with periodontitis stages II to IV
- Have bilateral deep periodontal pockets measuring 5 mm or more
You will not qualify if you...
- Limited mouth opening or symptomatic temporomandibular joint disorder
- Unable to tolerate extended periodontal treatment or have a hyperactive gag reflex
- Current or former smoker or vape user
- Pregnant or breastfeeding
- Have diabetes mellitus type I or II
- Have a bleeding disorder or are on anticoagulant medication
- Received periodontal treatment or surgery within the past 6 months
- Currently undergoing orthodontic therapy or completed it within the past 3 months
- Taken anti-inflammatory drugs in the past 3 months
- Taken antibiotics in the past 3 months
- Have an autoimmune disorder
- Taken immunosuppressant drugs in the past 3 months
- Undergoing or previously underwent radiation or chemotherapy
AI-Screening
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Trial Site Locations
Total: 1 location
1
Faculty of Dentistry, MAHSA University
Jenjarum, Selangor, Malaysia, 42610
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
2
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