Endodontic Micro-Surgery: Surgery performed using bone graft(DFDBA) and iPRF with collagen membrane in test group and bone graft and iPRF without collagen membrane in control group
Study summary
To determine the effect of allograft and iPRF with or without collagen membrane on healing of apicomarginal defects : A Randomized Controlled Trial
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
1. Patients with no general medical contraindications for oral surgical procedures (ASA-I and ASA-II according to the classification of the American Society of Anesthesiologist's).
2. Patients aged 18 years and above, presenting with chronic suppurative apical periodontitis in at least one tooth,
3. Radiographic evidence of apical radiolucency with periodontal pocket depth exceeding 6 mm confined to buccal aspect of the root.
4. Repeated abscess discharge despite satisfactory root canal treatment. 5.Patients with apicomarginal defects showing a denuded buccal bone plate
6.Failed primary root canal treatment 7.Adequate final restoration with no clinical evidence of coronal leakage.
Exclusion Criteria:
1. Clinical or radiographic evidence of root fracture.
2. Resorptive processes involving more than apical third of the root.
3. Chronic generalized periodontitis.
4. Failed previous endodontic surgery or failed root canal re-treatment.
5. Any systemic disease contraindicating oral surgery including uncontrolled diabetes and pregnancy, any condition effecting rate of healing like smoking.
Primary outcome measure(s)
Periapical healing assessment — Base line to 12 months Periapical healing comparison in 2 groups with buccal bone regeneration and 2d healing and 3d healing outcome using Rud and Molven et al. (1987). \& modified PENN 3D criteria .
Trial sites (1)
Facility
City
Region
Status
PGIDS
Rohtak
Haryana
Recruiting
More Postgraduate Institute of Dental Sciences Rohtak trials in India
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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