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. Author manuscript; available in PMC: 2006 Aug 28.
Published in final edited form as: Obstet Gynecol. 2005 Nov;106(5 Pt 1):946–952. doi: 10.1097/01.AOG.0000182576.48290.6d

Table 1.

Baseline Characteristics of 417 Ultra Low Dose Transdermal estRogen Assessment Participants by Treatment Group

Estradiol n = 20 Placebo n = 20 P*
Age 66.8 ± 5.1 66.7 ± 4.8 .96
Years since menopause 37.0 ± 5.1 37.4 ± 4.7 .57
White race 92.8 91.9 .45
Body mass index 28.3 ± 5.3 28.0 ± 5.3 .60
Parity 3.2 ± 1.7 3.3 ± 1.8 .70
Medical conditions
  Diabetes 3.4 1.0 .09
  Hypertension 16.4 14.8 .65
Current smoker 7.7 6.2 .55
Estradiol level in pg/mL [median (interquartile range)] 4.8 (2.7–8.0) 4.7 (2.7–8.3) .62
Weekly or more frequent incontinence
  Any type 41.3 44.0 .62
  Stress 25.0 27.5 .53
  Urge 26.0 25.8 1.00
Frequency of incontinence, episodes/wk
  None 58.6 56.5 .80
  1 16.8 16.9
  2–6 18.8 18.4
  ≥ 7 5.8 8.2
Incontinence type, mean episodes/wk
  Any 1.9 ± 6.9 1.7 ± 4.3 .57
  Stress 1.3 ± 6.0 1.1 ± 3.6 .47
  Urge 0.6 ± 1.8 0.7 ± 1.7 .84

SD, standard deviation.

Values are mean ± standard deviation or %, except where otherwise specified.

*

The P values for categorical variables were calculated using generalized Cochran-Mantel-Haenszel tests, stratified by clinic site. The P values for continuous variables are from analysis of variance or rank analysis of variance, adjusted for site.