Trial reportBMC oral health2026
Dentine-derived barrier membrane versus extended platelet-rich fibrin for guided bone regeneration: a 2-year randomized clinical trial.
Trial report in BMC oral health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07396350 (Autogenous Dentine Derived Barrier Membrane Versus Extended Platelet Rich Fibrin Membrane in Immediate Implant Placement in Posterior Mandible), which is not on this map. Not yet cited in PubMed.
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Autogenous Dentine Derived Barrier Membrane Versus Extended Platelet Rich Fibrin Membrane in Immediate Implant Placement in Posterior Mandible: a 2 Year Follow up
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4 authors.
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Abstract
backgroundAn autogenous dentine-derived barrier membrane (DDBM), primarily consisting of type I collagen, is a recognized as an osteo-conductive material in implant dentistry. A recently developed method is used to prolong the functional properties of PRF to 4 to 6 months. This newly prepared material is called Albumin-platelet rich fibrin (Alb-PRF) or extended platelet-rich fibrin (e-PRF). The aim of this study was to compare clinical and radiographic results of autogenous demineralized dentine-derived barrier membrane versus extended platelet-rich fibrin membrane for guided bone regeneration (GBR) with immediate implant placement in the posterior mandible. MATERIALS AND
methodsForty patients with non-restorable mandibular molars indicated for immediate implant placement and GBR were selected and randomly divided into two equal groups (n = 20 per group). In Group 1, implants were placed using a dentine-derived barrier membrane, while in Group 2, implants were placed using an extended platelet-rich fibrin membrane. All patients underwent clinical and radiographic assessments immediately after placement and at 3, 6, 12, and 24 months to evaluate implant stability, peri-implant probing depth (PPD), marginal bone loss (MBL), and relative bone density.
resultsAll implants achieved a 100% survival rate over the 24-month period. Implant stability increased significantly over time in both groups (P < 0.001), with no significant intergroup differences at any point; at 12 months, the median (IQR) was 78.0 (77.0-79) for Dentine Group and 79 (75.0-81.0) for e-PRF Group (P = 0.201, r = 0.207). PPD also increased significantly within both groups (P < 0.001), but remained within healthy limits, with no significant differences between groups at any points; at 24 months, the median (IQR) was 3.25 mm (3.13-3.50 mm) for Dentine Group vs. 3.25 mm (3.0-3.31 mm) for e-PRF Group; (P = 0.142, r = 0.241). MBL increased significantly over time in both groups (P < 0.001). At 24 months, no significant intergroup differences were found for buccal MBL, the median (IQR) was 1.22 mm (1.20-1.30 mm) for Dentine Group vs. 1.30 mm (1.25-1.39 mm) for e-PRF Group; P = 0.060, r = 0.300) or lingual MBL, the median (IQR) was 1.27 mm (1.20-1.37 mm) for Dentine Group vs. 1.27 mm (1.19-1.37 mm) for e-PRF Group; (P = 0.678, r = 0.069). Similarly, relative bone density showed a significant intragroup increase (P < 0.001) with no significant intergroup differences at 24 months for buccal density the median (IQR) was 1204.5 (1150.0-1261.0) for Dentine Group vs. 1266.0 (1119.0-1311.0) for e-PRF Group; (P = 0.183, r = 0.214) or lingual density the median (IQR) was 1180.0 (1156.0-1210) for Dentine Group vs. 1212.50 (1112.0-1233.0) for e-PRF Group; (P = 0.314, r = 0.163).
conclusionBoth autogenous DDBM and e-PRF membrane demonstrated favorable clinical and radiographic outcomes over 24 months when used for GBR in conjunction with immediate implant placement in the posterior mandible. Both materials represent cost-effective, biological alternatives for GBR, maintaining stable peri-implant tissues over a 2-year period.
trial registrationThe study was retrospectively registered at ClinicalTrials.gov PRS ( https://register. CLINICALTRIALS: gov ) under the identifier number NCT07396350 on 02/02/2026.
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