Clinical and Radiographic Evaluation of Using the Entire Papilla Preservation Technique With and Without Autogenous Bone Graft and Injectable Platelet Rich Fibrin in Treatment of Periodontal Intraosseous Defects
Launched by CAIRO UNIVERSITY · Mar 29, 2024
Trial Information
Current as of June 18, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at new ways to treat specific types of gum disease known as isolated intrabony periodontal defects. These are pockets of infection that can occur in the bone around teeth, particularly in patients with a more advanced stage of gum disease called stage III periodontitis. The study will compare two methods: one that uses a technique called the entire papilla preservation technique with and without adding a bone graft (using a piece of the patient's own bone) and an injectable treatment called platelet-rich fibrin, which may help the healing process.
To participate in this trial, you need to be an adult aged 18 or older with a healthy overall health condition and a specific type of gum problem that meets certain criteria, including having a deep pocket around one tooth. Participants must also maintain good oral hygiene and be willing to follow up for six months. If you are taking medications that could affect your gum disease, are a heavy smoker, or are pregnant, you may not be eligible. If you qualify and choose to participate, you can expect to receive treatment and regular check-ups to monitor your progress and the health of your gums.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients with healthy systemic condition.
- • 2. Adult patients (18 years old and older).
- • 3. Patients with stage lll periodontitis, having one isolated intrabony defect with probing depth \>6mm, clinical attachment level\> 6mm and at least 4 mm intrabony component involving predominantly the interproximal area of the affected tooth.
- • 4. Patients with full mouth plaque score\<20%.
- • 5. Patients with full mouth bleeding score\<20%.
- • 6. Compliance with good oral hygiene.
- • 7. Patients accept 6-months follow-up period (cooperative patients).
- • 8. Patients provide an informed consent.
- Exclusion Criteria:
- • 1. Ongoing drug therapy that might have an impact on the clinical signs and symptoms of periodontitis.
- • 2. One wall intrabony defect.
- • 3. Defects that involve the buccal and lingual sites.
- • 4. Smokers ˃ 10 cigarettes / day.
- • 5. Pregnant and lactating females.
About Cairo University
Cairo University, a premier institution in Egypt, is dedicated to advancing medical research and education through innovative clinical trials. With a strong emphasis on improving healthcare outcomes, the university collaborates with various stakeholders to conduct rigorous scientific studies that address critical health challenges. Leveraging its extensive resources and expert faculty, Cairo University aims to contribute valuable insights to the medical community and enhance patient care both locally and globally. Through its commitment to ethical research practices and excellence, the university plays a pivotal role in shaping the future of healthcare in the region.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Cairo, , Egypt
Patients applied
Trial Officials
Laila T Sedeek, Bachelor
Principal Investigator
Cairo University
Manal M Hosny, Professor
Study Director
Cairo University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported