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Exact(60)
Ninety patients were randomised into two treatment groups.
Patients were randomised to receive either 4 mg q.d.
Patients were randomised between any intervention according to therapeutic strategy or standard medical treatment.
Patients were randomised to receive 100 μg pTVG-HP with 200 μg rhGM-CSF i.d.
The patients were randomised by computer and allocated to two groups: intervention and control.
Patients were randomised to gabapentin (n=153) or placebo (n=152).
Sixty-three patients were randomised to receive sativex and 62 placebo.
Subsequent patients were randomised to receive either continuous PC6 acupressure or placebo acupressure.
From 1995 to 2002, 138 patients were randomised between the two groups.
Patients were randomised to either enhanced physiotherapy or standard care groups as part of a larger RCT.
Patients were randomised in blocks of ten to receive either MAS3 or DHA-PPQ.
More suggestions(17)
hospitals were randomised
adolescents were randomised
parents were randomised
practitioners were randomised
participants were randomised
infants were randomised
clients were randomised
neonates were randomised
recipients were randomised
clinics were randomised
subjects were randomised
respondents were randomised
patients were evacuated
patients were rounded
patients were treated
patients were studied
patients were left
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