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Table 1 Baseline characteristics of study participants in the piroxicam (PRX) and the placebo (PLC) groups

From: Effect of sublingual fast-dissolving piroxicam premedication on postoperative pain experience in mandibular molars with non-vital pulp: a randomized double-blind controlled trial

Variable

Categories

PRX

(n = 35)

PLC

(n = 35)

P-Value

Age

Mean ± SD

32.66 (10.30)

33.4 (9.95)

0.76

Median

33

32

(Min- Max)

(19—60)

(18—60)

Sex

Males [n (%)]

10 (28.6)

17 (48.6)

0.086

Females [n (%)]

25 (71.4)

18 (51.4)

Molar Type

1st [n (%)]

26 (74.3)

25 (71.4)

0.788

2nd [n (%)]

9 (25.7)

10 (28.6)

Number of canals

3 [n (%)]

30 (85.7)

25 (82.9)

0.743

4 [n (%)]

5 (14.3)

10 (17.1)

Periapical lesion size

0-2 mm [n (%)]

20 (57.1)

21 (60.0)

0.143

 > 2-5 mm [n (%)]

15 (42.9)

14 (40.0)

Last food intake

 ≥ 8 h (Fast) [n (%)]

14 (40.0)

13 (37.1)

0.806

 < 8 h (Ate) [n (%)]

21 (60.0)

22 (62.9)

MDAS

 ≥ 12 (Anxious) [n (%)]

 < 12 (Calm) [n (%)]

22 (62.9)

13 (37.1)

16 (45.7)

19 (54.3)

0.150

  1. Max Maximum, MDAS Modified Dental Anxiety Scale, Min Minimum, SD, Standard deviation