<p>Supplementary Table ST1: Results of clinical, histological and combined response evaluation Supplementary Table ST2: Results of clinical response only in patients who have 6 month clinical evaluation completed. Supplementary Table ST3: Summary of association between Clinical and Histological response at 6 months for Curcumin group Supplementary Table ST4: Result of longer-term treatment in subjects with partial response. Supplementary Table ST5: Number and Percentage of Patients with Treatment-Emergent Adverse Events during the Study (Safety Population) Supplementary Table ST6: Summary of results of two systematic review and meta-analysis of chemoprevention trial of oral leukoplakia (26, 27).</p>
<p>Supplementary Table ST1: Results of clinical, histological and combined response evaluation Supplementary Table ST2: Results of clinical response only in patients who have 6 month clinical evaluation completed. Supplementary Table ST3: Summary of association between Clinical and Histological response at 6 months for Curcumin group Supplementary Table ST4: Result of longer-term treatment in subjects with partial response. Supplementary Table ST5: Number and Percentage of Patients with Treatment-Emergent Adverse Events during the Study (Safety Population) Supplementary Table ST6: Summary of results of two systematic review and meta-analysis of chemoprevention trial of oral leukoplakia (26, 27).</p>
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