Non-Cochrane · intervention · PM41585592

Comparative success of platelet-rich fibrin and mineral trioxide aggregate in direct pulp capping and pulpotomy: a systematic review and meta-analysis.

Alkabazi Malik, Aldieb Ebtesam · Biomaterial investigations in dentistry · 2026 · PubMed · doi:10.2340/biid.v13.45302

Findings

12 findings

Population
Adults or children with pulpitis (reversible or irreversible) requiring direct pulp capping or pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Overall (common-effect model)
OR 0.77 [0.44, 1.34]
GRADE not reported
7 studies · 436 participants
Adults or children with pulpitis (reversible or irreversible) requiring direct pulp capping or pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Overall (common-effect model)
OR 1.51 [0.94, 2.43]
GRADE not reported
7 studies · 392 participants
Adults or children with pulpitis (reversible or irreversible) requiring direct pulp capping or pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Overall (random-effects model)
OR 1.5 [0.93, 2.43]
9 [-2, 18] per 100
Low
Downgraded: risk of bias, imprecision
7 studies · 392 participants
Adults or children with pulpitis (reversible or irreversible) requiring direct pulp capping or pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Overall (random-effects model)
Unresolved: the two extractors disagree on this row.
OR 0.72 [0.29, 1.78]
-5 [-23, 6] per 100
Low
Downgraded: imprecision
7 studies · 436 participants
Patients requiring direct pulp cappingPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Procedure: pulp capping; Common-effect model
OR 1.45 [0.65, 3.2]
GRADE not reported
4 studies · 212 participants
Patients requiring direct pulp cappingPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Procedure: pulp capping; Random-effects model
OR 2.4 [0.53, 10.87]
GRADE not reported
3 studies · 198 participants
Patients requiring direct pulp cappingPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Procedure: pulp capping; Random-effects model
OR 1.44 [0.64, 3.22]
GRADE not reported
4 studies · 212 participants
Patients requiring direct pulp cappingPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Procedure: pulp capping; Common-effect model
OR 3.38 [1.1, 10.38]
GRADE not reported
3 studies · 198 participants
Patients requiring pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Procedure: pulpotomy; Random-effects model
OR 0.41 [0.18, 0.93]
GRADE not reported
4 studies · 238 participants
Patients requiring pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Procedure: pulpotomy; Common-effect model
OR 1.54 [0.85, 2.8]
GRADE not reported
3 studies · 180 participants
Patients requiring pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
6 months · Procedure: pulpotomy; Common-effect model
OR 0.36 [0.17, 0.76]
GRADE not reported
4 studies · 238 participants
Patients requiring pulpotomyPlatelet-rich fibrin (PRF), alone or combined with other materialsMineral trioxide aggregate (MTA)Clinical success (absence of symptoms, abnormal responses and radiographic signs)
12 months · Procedure: pulpotomy; Random-effects model
OR 1.54 [0.85, 2.8]
GRADE not reported
3 studies · 180 participants

Included primary studies 9

Open in Studies
StudyYearAlso included byOutcomes it informs hereTrial data
Keswani 2014
Comparative evaluation of platelet-rich fibrin and mineral trioxide aggregate as pulpotomy agents in permanent teeth with incomplete root…
PMID:24767550
20142 other reviewsClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Kumar 2016
Comparative evaluation of platelet-rich fibrin, mineral trioxide aggregate, and calcium hydroxide as pulpotomy agents in permanent molars…
PMID:27994420
20162 other reviewsClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Abuhashema 2025
Clinical and radiographic assessment of mineral trioxide aggregate with platelet rich fibrin as pulp capping biomaterials: a 12-month…
PMID:40234535
2025this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Eid 2022
Effectiveness of Three Agents in Pulpotomy Treatment of Permanent Molars with Incomplete Root Development: A Randomized Controlled Trial.
PMID:35326909
2022this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Manhas 2019
Biological approach in repair of partially inflamed dental pulp using second-generation platelet-rich fibrin and mineral trioxide…
PMID:31710016
2019this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Patidar 2017
Clinical and radiographic comparison of platelet-rich fibrin and mineral trioxide aggregate as pulpotomy agents in primary molars.
PMID:28914251
2017this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Shobana 2022
Efficacy of Platelet Rich Plasma and Platelet Rich Fibrin for Direct Pulp Capping in Adult Patients with Carious Pulp Exposure- A…
PMID:35786576
2022this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Singh 2020
To Compare Mineral Trioxide Aggregate, Platelet-rich Fibrin, and Calcium Hydroxide in Teeth with Irreversible Pulpitis: A Clinical Study.
PMID:33149501
2020this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet
Tiwari 2024
To Evaluate and Compare Platelet-rich Fibrin and Mineral Trioxide Aggregate as Direct Pulp Capping Agents in Primary Molars: A Randomized…
PMID:39185252
2024this review onlyClinical success (absence of symptoms, abnormal responses and radiographic signs)not extracted yet

Overlap with other reviews

Reviews that include the same primary studies are not independent evidence. Shared counts match studies by PMID, DOI or NCT, and otherwise by author and year (a probable match). Only the non-Cochrane dental reviews have study lists, so overlap with Cochrane reviews is not counted yet.

Review question

ElementPlanned (methods)Found (results)
PopulationAdults or children with symptomatic or asymptomatic reversible or irreversible pulpitis requiring direct pulp capping or pulpotomyPatients needing pulp capping (n=4 studies) or pulpotomy (n=5 studies); primary and permanent teeth; 5 to 45 years
InterventionPlatelet-rich fibrin alone or combined with other materialsPRF (alone or with MTA or Ca(OH)2) (n=9)
ComparisonMineral trioxide aggregateMTA (n=9); also Ca(OH)2, nano-hydroxyapatite, PRP in some trials
OutcomesSuccess rate (absence of spontaneous pain, abnormal thermal response, tenderness, swelling or sinus tract, radiographic evidence)Clinical success at 6 months (n=7 studies, 436 teeth) and 12 months (n=7 studies, 392 teeth)
Study designsRandomized and non-randomized clinical trials8 RCTs and 1 non-randomized clinical trial
TimingMinimum follow-up 6 monthsFollow-up 6, 12 and up to 24 months