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Primary outcome: The primary outcome measures were change in HbA1c, peal VO2, and biochemical analyses in T2D patients after a 12-week concurrent ET program.
Primary outcome measures were change in monthly migraine days and 50% responder rate, i.e. the percentage of subjects having a ≥ 50% reduction of monthly migraine days.
The main outcomes measures were change in uterine bleeding symptoms measured on a continuous and ordinal scale, patient satisfaction, time of work and use of health service resources at 6 months following treatment.
The main outcome measures were change in HbA1c and body weight, and final insulin dose.
21 To evaluate likely effectiveness, the primary outcome measures were change in PA levels and variety.
Primary outcome measures were change in BMI kg/m and BMI SD score after 2 years.
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Additional outcome measures were changes in PPT, 5-HT platelet poor plasma (P-5-HT), as well as pain distribution.
Primary outcome measures were changes in the JFK Coma Recovery Scale-Revised (CRS-R) scale total score and Clinical Global Impression Improvement (CGI-I) scale.
Primary outcome measures were changes in body composition, and metabolic abnormalities, secondary outcome measures were virologic and immunologic efficacy and overall safety.
The main outcome measures were changes in sexual activity, condom use and numbers of partners.
The main outcome measures were changes in BCVA and central retinal thickness (CRT).
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