Evidence map›Paper›PMID 42542468›Full record

Trial reportEvidence-based dentistry2026

Adult tooth regeneration: can blood beat biomaterials?

Casper Jonker

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Evidence-based dentistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Casper JonkerFaculty of Health, Peninsula Dental School, University of Plymouth, Plymouth, UK. casper.jonker@plymouth.ac.uk.ORCID http://orcid.org/0000-0002-9110-5208

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

a commentary onAwawdeh L, Almesleh B, Hammouri H, Al-Qudah A. The outcome of pulp revascularization of necrotic mature permanent teeth with periapical lesions using platelet-rich fibrin versus induced bleeding: a prospective preliminary randomized clinical trial. Clinical Oral Investigations. 2026; https://doi.org/10.1007/s00784-026-06877-w .

designA single-centre, prospective, two-arm parallel randomised clinical trial presented as a preliminary (early-phase) investigation. CASE SELECTION: Fifty adults presenting with mature permanent teeth where the pulpal status was diagnosed as necrotic with associated periapical lesions were included. The pool of patients was allocated to one of two regenerative endodontic treatment protocols, each containing 25 patients. In one group, 25 patients underwent a procedure where a canal scaffold was generated by deliberately provoking bleeding from the periapical tissues (induced bleeding, IB). In the second group of patients, an autologous platelet-rich fibrin (PRF) membrane was placed to serve as a biological barrier. A clinical and radiographic review was done at baseline, 6 months, and 12 months after treatment completion. DATA ANALYSIS: Pre-specified endpoints were set to determine, firstly, tooth survival and overall treatment success and secondly, periradicular healing through radiographic evaluation. Within- and between-group comparisons were made using the appropriate statistical tests and statistical significance was set at p < 0.05.

resultsAt the one-year mark, 98% of teeth had survived (47/48). Interestingly, survival did not differ meaningfully between the two treatment groups (p = 0.166). Both treatment options produced healing with a statistically significant reduction in periradicular pathology compared with baseline at the six- and twelve-month reviews (p < 0.001). Also, a statistically significant impact was found on the overall success rate at the endpoint (p = 0.022). In the IB group, a 100% success rate was achieved (23/23) compared to 75% in the PRF group (18/24), with a combined overall success of 85.4%.

conclusionsWhichever treatment pathway was followed, all teeth survived the chosen regenerative endodontic procedure after 12 months. The preliminary results indicated that results and clinical outcomes were comparable. Although the IB option showed a higher overall success rate, this finding should be interpreted with caution as the results fall within the early phase clinical evidence framework. Further investigations are required to determine the superiority of one method over the other.

Indexed as

Biocompatible MaterialsDental Pulp NecrosisPlatelet-Rich FibrinRegenerationRegenerative EndodonticsAdultFemaleHumansProspective StudiesBiocompatible Materials

Identifiers

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.