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Table 1 Demographics and baseline characteristics

From: A 4-week, dose-ranging study comparing the efficacy, safety and tolerability of latanoprost 75, 100 and 125 μg/mL to latanoprost 50 μg/mL (xalatan) in the treatment of primary open-angle glaucoma and ocular hypertension

Latanoprost concentration (μg/mL)

 

50

75

100

125

ITT Population, N

71

70

72

69

Sex, n (%)

 Male

32 (45.1)

35 (50.0)

42 (58.3)

35 (50.7)

 Female

39 (54.9)

35 (50.0)

30 (41.7)

34 (49.3)

Race, n (%)

 Caucasian

56 (78.9)

57 (81.4)

55 (76.4)

56 (81.2)

 Black

1 (1.4)

0 (0)

2 (2.8)

1 (1.4)

 Asian

14 (19.7)

13 (18.6)

15 (20.8)

12 (17.4)

Age (years)

 Mean ± SD

59.5 ± 12.8

59.5 ± 12.0

60.6 ± 13.8

61.2 ± 12.7

 Median

61.0

59.0

60.5

63.0

 Range

20-82

26-85

20-85

26-89

Study eye, n (%)

 Right

16 (22.5)

15 (21.4)

13 (18.1)

11 (15.9)

 Left

8 (11.3)

8 (11.4)

11 (15.3)

16 (23.2)

 Both

47 (66.2)

47 (67.1)

48 (66.7)

42 (60.9)

Treated eye, n (%)

 Right

7 (9.9)

5 (7.1)

3 (4.2)

4 (5.8)

 Left

1 (1.4)

1 (1.4)

2 (2.8)

4 (5.8)

 Both

63 (88.7)

64 (91.4)

67 (93.1)

61 (88.4)

Worse eye, n (%)

 Right

50 (70.4)

43 (61.4)

39 (54.2)

36 (52.2)

 Left

21 (29.6)

27 (38.6)

33 (45.8)

33 (47.8)

Eye color, n (%)

 Homogenous blue, gray or green

8 (11.3)

11 (15.7)

4 (5.6)

11 (15.9)

 Homogenous brown

45 (63.4)

43 (61.4)

46 (63.9)

40 (58.0)

 Blue-brown or gray-brown

10 (14.1)

12 (17.1)

11 (15.3)

11 (15.9)

 Green-brown

4 (5.6)

3 (4.3)

8 (11.1)

4 (5.8)

 Yellow-brown

3 (4.2)

1(1.4)

3 (4.2)

3 (4.3)

 Different*

1 (1.4)

0 (0.0)

0 (0.0)

0 (0.0)

Diagnosis , n (%)

 Primary open-angle glaucoma

53 (74.6)

44 (62.9)

47 (65.3)

47 (68.1)

 Ocular hypertension

16 (22.5)

18 (25.7)

21 (29.2)

16 (23.2)

 Different*

2 (2.8)

8 (11.4)

4 (5.6)

6 (8.7)

IOP-lowering medication at

screening, n%

 Alpha agonists

3 (4.2)

5 (7.1)

6 (8.3)

1 (1.4)

 Beta-blockers

33 (46.5)

28 (40.0)

26 (36.1)

23 (33.3)

 Carbonic anhydrase inhibitors

7 (9.9)

8 (11.4)

2 (2.8)

2 (2.9)

 Combination drugs

9 (12.7)

6 (8.6)

4 (5.6)

5 (7.2)

 Parasympathomimetics

0 (0.0)

1 (1.4)

0 (0.0)

2 (2.9)

 Prostaglandins

23 (32.4)

19 (27.1)

20 (27.8)

20 (29.0)

 Sympathomimetics

1 (1.4)

1 (1.4)

0 (0.0)

0 (0.0)

PP Population, N

69

66

71

68

Baseline IOP

Worse eye8 a.m.

 Mean ± SD

26.9 ± 3.1

26.6 ± 3.0

26.5 ± 2.5

26.8 ± 2.8

 Range

24.0 – 36.0

24.0 – 36.0

24.0 – 35.0

24.0 – 36.0

4 p.m.

 Mean ± SD

25.3 ± 3.6

24.6 ± 3.5

25.3 ± 3.1

25.7 ± 3.7

 Range

16.5 – 37.0

15.0 –35.0

17.5 – 34.0

18.0 – 36.0

Study eye

8 a.m.

 Mean ± SD

26.5 ± 2.8

26.1 ± 2.5

26.2 ± 2.4

26.4 ± 2.4

 Range

24.0 – 34.0

24.0 – 36.0

24.0 – 35.0

24.0 – 34.0

4 p.m.

 Mean ± SD

25.1 ± 3.4

24.3 ± 3.1

25.1 ± 2.9

25.3 ± 3.3

 Range

16.5 – 35.0

15.5 – 34.0

18.0 – 34.0

18.0 – 36.0

  1. IOP intraocular pressure, ITT intention-to-treat, PP per protocol, SD standard deviation.
  2. *If the diagnosis/eye color of a subjects eye was not the same in both eyes, the outcome was given as different.
  3. By subject (i.e. diagnoses for both eyes of the subject were combined).