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The primary analysis was done using mixed model linear regression analysis comparing baseline worst fatigue on the BFI with worst fatigue after being randomized to either L-carnitine or placebo.
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Between August 2002 and January 2005, a randomized controlled trial was conducted, in which women were randomized to either abdominal or laparoscopic hysterectomy.
Mothers were randomized to either propofol or isoflurane anaesthesia.
After inclusion, patients were randomized to either FreeO2 or conventional O2 manual adjustment during 3 hours.
Methods: Ninety patients having open vein stripping were randomized to either sevoflurane or propofol anesthesia.
Animals were randomized to either nalbuphine or placebo (NaCl 0.9%) infusions.
After successful reduction, patients were randomized to either externally or internally rotated immobilization.
Patients are randomized to either forced fluid removal or standard care for the entire ICU stay.
Seventy-three participants (68.5% women) were randomized to either ACT or treatment as usual (TAU).
Only those able to maintain euthymia for 4 successive weeks (app. 120) will be randomized to either SBAA+ or SBAA.
A total of 875 patients were randomized to either fremanezumab quarterly (N=291), fremanezumab monthly (N=290) or placebo (N=294).
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CEO of Professional Science Editing for Scientists @ prosciediting.com