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. 2023 Feb 14;15(2):643. doi: 10.3390/pharmaceutics15020643

Table 4.

The primary outcome measure based on VAS score for lower abdominal pain, lower backache (LBA), and Modified McCormack (McPS) for pelvic tenderness.

VAS for Lower Abdominal Pain Pessary Group (n = 33) Standard Group (n = 33) p-Value
D0 3.45 ± 2.21 3.58 ± 2.65 0.841
D7 1.85 ± 1.46 1.97 ± 1.78 0.763
D14 0.67 ± 0.89 * 0.82 ± 1.33 ** 0.589
D30 0.18 ± 0.46 * 0.52 ± 1.09 ** 0.112
%Pain Reduction (PR) 80.57% 77.09%
VAS for lower back ache
D0 2.48 ± 2.29 3.55 ± 2.69 0.090
D7 1.42 ± 1.44 2.18 ± 1.98 0.080
D14 0.64 ± 0.93 * 1.12 ± 1.47 ** 0.115
D30 0.27 ± 0.63 * 0.64 ± 1.08 ** 0.100
% Pain Reduction PR 74.19% 68.54%
Modified McCormack Pain Scale (McPS) for pelvic tenderness
D0 3.82 ± 1.59 3.76 ± 1.50 0.874
D7 2.52 ± 1.20 2.55 ± 1.00 0.912
D14 0.94 ± 1.00 * 1.21 ± 1.11 ** 0.298
D30 0.42 ± 0.66 * 0.73 ± 1.01 ** 0.154
% Pain Reduction (PR) 75.39% 67.81%

* p < 0.001 and ** p < 0.001 on day 14 and day 30 from day 0 in the pessary group and standard group respectively; unpaired ‘t’ test and paired ‘t’ test; % PR: % pain reduction at day 14 compared to day 0.