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MeSH Review

Cross-Over Studies

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Disease relevance of Cross-Over Studies


Psychiatry related information on Cross-Over Studies


High impact information on Cross-Over Studies

  • Ten women whose symptoms improved during leuprolide treatment were given estradiol and progesterone in a double-blind, crossover design, each for four weeks, during continued leuprolide administration [11].
  • METHODS: In a randomized, crossover study, we investigated the effects of oral conjugated estrogen (0.625 mg per day) in 30 postmenopausal women and transdermal estradiol (0.1 mg per day) in 20 postmenopausal women, either alone or in combination with medroxyprogesterone acetate (2.5 mg daily) for one month, on plasma PAI-1 antigen levels [12].
  • In a double-blind crossover study, the patients received theophylline or placebo orally twice daily for five days, with one week of washout between the two periods [13].
  • On days 3 through 5 the subjects were pretreated with 4 ml of inhaled heparin (1000 U per kilogram), cromolyn sodium (20 mg), or placebo according to a single-blind, randomized, crossover design and underwent exercise challenge 45 minutes later [14].
  • In a randomized, double-blind, crossover study, 12 patients with mild asthma each inhaled a single dose of terbutaline (500 micrograms) or placebo before a challenge with a series of doubling doses of inhaled methacholine or AMP, before and after treatment for seven days with 500 micrograms of terbutaline four times daily or placebo [15].

Chemical compound and disease context of Cross-Over Studies


Biological context of Cross-Over Studies


Anatomical context of Cross-Over Studies


Associations of Cross-Over Studies with chemical compounds


Gene context of Cross-Over Studies


Analytical, diagnostic and therapeutic context of Cross-Over Studies


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