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A Study to Compare and evaluate the effect of one sided gum surgery alone or in combination with Component of blood (PRF) in bony defects associated with gum disease.

A clinical and radiographic evaluation of modified single buccal flap approach and its coronal respositioning with and without platelet rich fibrin (PRF) in periodontal intrabony defects- A double blind randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021752
Enrollment
32
Registered
2019-10-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K053- Chronic periodontitis Health Condition 2: null- Periodontitis (osseous defects)

Interventions

Intervention1: Group B: Single buccal flap with platelet rich fibrin in treatment of periodontal intrabony defects Control Intervention1: Group A: Single buccal flap alone in treatment of periodontal

Sponsors

MIDSR Dental college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient diagnosed with localized or generalized chronic periodontitis as per American Academy of Periodontology International Workshop for Classifications of Periodontal Disease 1999. 2. Subjects having acceptable systemic health. 3. Intrabony defect in both maxillary or mandibular region. 4. Patients having at least one intrabony defect more than or equal to 3 mm along with attendant pocket depth more than or equal to 5mm. 5. Absence of overt clinical inflammation at the time of surgery. 6. Patient signing written informed consent

Exclusion criteria

Exclusion criteria: 1. Medically compromised patients. 2. With unacceptable oral hygiene (Plaque index >2) 3. With any metabolic disease or endocrine disease having direct or indirect influence on Bone healing. 4. With any periapical pathology associated with endodontic infection in the region of Interest. 5. Patient on active orthodontic treatment. 6. Patient having >4 mm pocket in selected tooth on mid oral or palatal aspect, requiring Buccal as well as oral flap for access. 7. Pregnant and lactating women. 8. Presence of defective prosthesis in the area of interest. 9. Subjects who are smokers and consume tobacco in any form. 10. Patient who are using drugs that may cause gingival enlargement, those allergic or sensitive to any medications that will be used in the study.

Design outcomes

Primary

MeasureTime frame
Probing depth, Clinical attachment level Radiographic bone fill Timepoint: At 3 month and at 6 months—

Secondary

MeasureTime frame
Gingival marginal level, plaque index, gingival indexTimepoint: At 3month and at 6 months—

Countries

India

Contacts

Public ContactDr Omkumar Baghele

MIDSR DENTAL COLLEGE LATUR

salim0007dx15@gmail.com8421599981

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026