| Literature DB >> 27965713 |
Yingming Yang1, Tao Zhang1, Zibo Dong2, Yang Wu1, Xiao Hong1, Tao Hu1.
Abstract
Aim. To examine the potential of Pudilan Keyanning toothpaste (PKT) to treat minor aphthous ulcers (MiAU). Method. A double-blind clinical trial was conducted in which 80 volunteers were randomly assigned to the PKT group (N = 40) or the control group (N = 40). The control group used a placebo toothpaste containing no Pudilan extract. At baseline, after 3 days, and after 6 days the following parameters were recorded for the target ulcers: healing rate, healing period, pain (visual analogue scale, VAS), areas of the target ulcerated lesions, degree of exudation, and hyperemia. Results. At the end of the study, the healing rate in the PKT group was 80%, compared to 50% in the control group (p < 0.05). At day 6, the VAS scores, ulcer area, degree of exudation, and hyperemia were significantly different between the two groups, with better performance observed in the PKT group (p < 0.05). Conclusion. PKT toothpaste appears to promote effective healing of MiAU.Entities:
Year: 2016 PMID: 27965713 PMCID: PMC5124687 DOI: 10.1155/2016/9125327
Source DB: PubMed Journal: Evid Based Complement Alternat Med ISSN: 1741-427X Impact factor: 2.629
Superiority test of the healing rate in the two groups.
| Group |
| Target ulcer healed | Target ulcer not healed | Healing rate (%) | 95% CI (HO: T − C ≤ 0) |
|
|---|---|---|---|---|---|---|
| Study | 40 | 32 | 8 | 80 | [0.125, +∞] | 0.002 |
| Control | 40 | 20 | 20 | 50 | ||
|
| ||||||
| Control | 40 | 20 | 20 | 50 | [−0.475, +∞] | 0.998 |
| Study | 40 | 32 | 8 | 80 | ||
VAS scores of the PKT and control groups.
| Time of measurement | Group |
| Mean | Std | 95% CI |
|
|---|---|---|---|---|---|---|
| Day 3 | Study | 40 | 3.08 | 1.99 | 2.46–3.69 | 0.2147 |
| Control | 40 | 2.58 | 2.26 | 1.87–3.28 | ||
|
| ||||||
| Day 6 | Study | 40 | 0.43 | 1.13 | 0.075–0.78 | 0.0156 |
| Control | 40 | 1.13 | 1.77 | 0.576–1.674 | ||
Figure 1VAS scores of the PKT and control groups measured each day.
Figure 2VAS scores of the PKT and control groups at two follow-ups.
Comparison of the ulcerous area in the PKT and control groups.
| Time of measurement | Group |
| Mean | Std | 95% CI | Wilcoxon |
|---|---|---|---|---|---|---|
| Day 3 | Study | 40 | 6.68 | 6.55 | 4.65–8.71 | 0.9885 |
| Control | 40 | 8.67 | 9.48 | 5.73–11.60 | ||
|
| ||||||
| Day 6 | Study | 40 | 1.98 | 4.76 | 0.50–3.45 | 0.0108 |
| Control | 40 | 4.91 | 8.69 | 2.22–7.61 | ||
Figure 3Target ulcer areas of the PKT and control groups at two follow-ups.
Comparison of the degree of exudation and hyperemia in the PKT and control groups.
| Time of measurement | Score | Number of volunteers (% of the group) | Wilcoxon test | ||
|---|---|---|---|---|---|
| Study group | Control group | ||||
| Exudation | Day 3 | 0 | 3 (7.5%) | 9 (22.5%) | 0.9471 |
| 1 | 11 (27.5%) | 6 (15.0%) | |||
| 2 | 21 (52.5%) | 15 (37.5%) | |||
| 3 | 5 (12.5%) | 10 (25.0%) | |||
| Day 6 | 0 | 32 (80.0%) | 22 (55.0%) | 0.0180 | |
| 1 | 3 (7.5%) | 7 (17.5%) | |||
| 2 | 5 (12.5%) | 9 (22.5%) | |||
| 3 | 0 (0%) | 2 (5.0%) | |||
|
| |||||
| Hyperemia | Day 3 | 0 | 6 (15.0%) | 8 (20.0%) | 0.7803 |
| 1 | 21 (52.5%) | 19 (47.5%) | |||
| 2 | 13 (32.50%) | 13 (32.5%) | |||
| 3 | 0 (0%) | 0 (0%) | |||
| Day 6 | 0 | 33 (82.5%) | 22 (55.0%) | 0.0100 | |
| 1 | 6 (15.0%) | 16 (40.0%) | |||
| 2 | 0 (0%) | 2 (5.0%) | |||
| 3 | 1 (2.5%) | 0 (0%) | |||
Comparison of degree of compliance in the two groups.
| Group |
| Mean | Min | 25th percentile | 75th percentile | Max | Std | 95% CI | Wilcoxon |
|---|---|---|---|---|---|---|---|---|---|
| Study | 40 | 100.2 | 91.7 | 100.0 | 100.0 | 116.6 | 3.510 | 99.1–101.3 | 0.1701 |
| Control | 40 | 101.0 | 83.3 | 100.0 | 100.0 | 116.7 | 5.056 | 99.5–102.6 |