Trial reportMedical science monitor : international medical journal of experimental and clinical research2025
Comparative Analysis of Gelatin/Polylactic Acid and Commercial PLA Membranes for Guided Bone Regeneration: A Randomized Clinical Trial.
Trial report in Medical science monitor : international medical journal of experimental and clinical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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.
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.
Who cites it
1 citing paper in PubMed.
- Rapid neuralized and vascularized osteogenesis in infected bone defect using biomimetic biomineralized and antibacterial hydrogels.Frontiers in bioengineering and biotechnology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND This study included 32 patients with single missing teeth and alveolar bone defects and aimed to compare outcomes from guided bone regeneration with a gelatin/polylactic acid (GT/PLA) barrier membrane and a Guidor® bioresorbable matrix barrier dental membrane. MATERIAL AND METHODS A total of 32 participants were recruited in the clinical study, with single missing teeth and alveolar bone defects, requiring guided bone regeneration (32 missing teeth in total). They were randomly divided into the GT/PLA membrane group (experimental) and Guidor® membrane group (control) by the envelope method (n=16). Both membranes were used intraoperatively to cover the bone substitute material. Cone beam computed tomography (CBCT) was performed immediately and at 6 months after surgery to assess the amount of bone resorption. In addition, the osteogenic efficacy was calculated. The soft tissue index (STI), wound healing, membrane exposure, and incidence of infection in the operative area were evaluated. RESULTS The implant survival rate was 100% in both groups. The average bone resorption was 148.54±107.42 mm³ in the experimental group and 185.25±85.31 mm³ in the control group (P=0.163); the osteogenic efficacy was 75% in the experimental group and 56% in the control group (P=0.458). Moreover, the parameters of STI, wound healing, membrane exposure, and incidence of infection in the operative area showed no statistically significant difference between the 2 groups (P>0.05). CONCLUSIONS The GT/PLA barrier membrane yielded non-inferior clinical and imaging results to the GUIDOR® membrane, exhibiting good efficacy and biocompatibility in GBR.
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Registered trials
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