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        <identifier>oai:figshare.com:article/33979918</identifier>
        <datestamp>2026-09-24T05:33:10Z</datestamp>
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          <dc:title>Table 2_Clinical trials on 3D bioprinted scaffolds for lower extremity vascular, diabetic and pressure ulcers: a systematic review.docx</dc:title>
          <dc:creator>Lok Lam Lorraine Cheng (25102228)</dc:creator>
          <dc:creator>Chun Chit Cheung (25102231)</dc:creator>
          <dc:creator>Yiu Che Chan (14802419)</dc:creator>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>3D bioprinting</dc:subject>
          <dc:subject>lower extremity ulcers</dc:subject>
          <dc:subject>regenerative medicine</dc:subject>
          <dc:subject>scaffold</dc:subject>
          <dc:subject>ulcers</dc:subject>
          <dc:description>Aim&lt;p&gt;Three-dimensional (3D) bioprinting enables fabrication of bioink-based scaffolds that mimic native tissue architecture. This systematic review aims to evaluate the safety profile and healing times of 3D-bioprinted scaffolds clinically tested in human lower limb ulcers.&lt;/p&gt;Methods&lt;p&gt;A systematic review was conducted in accordance with PRISMA guidelines. PubMed, Embase, Scopus, and Web of Science were searched from January 2000 to June 2025. Inclusion criteria encompassed only clinical studies; animal, in vitro, and non-clinical reports were excluded. Risk of bias was assessed using the revised Cochrane risk-of-bias tool for randomized trials (RoB 2) for randomized controlled trials and the Methodological Index for Non-Randomized Studies (MINORS) for non-randomized studies. Results were synthesized narratively due to clinical and methodological heterogeneity across studies.&lt;/p&gt;Results&lt;p&gt;Of 476 records screened, eight studies met the inclusion criteria: two randomized controlled trials and six single-arm studies. The combined sample size across all studies was 139 patients. Both RCTs reported a statistically significant reduction in time to complete epithelialization versus standard dressings. In the single-arm studies, &gt;80% of ulcers achieved complete epithelialization within 12 weeks. No treatment-related serious adverse events were reported. Risk-of-bias assessments identified methodological limitations across studies (variable randomization and blinding, small sample sizes, and limited follow-up).&lt;/p&gt;Conclusion&lt;p&gt;Current clinical evidence indicates that 3D-bioprinted scaffolds, particularly Autologous Minimally Manipulated Homologous Adipose Tissue (AMHAT) and polylactic-acid gelatin constructs, represent a promising and apparently safe approach to accelerate ulcer healing and improve cosmetic outcomes. However, the number of patients included in each study were small with relatively short follow-up. Larger, high-quality randomized trials with longer follow-up are needed to confirm efficacy and long-term safety.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-24T05:33:10Z</dc:date>
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          <dc:identifier>10.3389/fbioe.2026.1912135.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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