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The randomization centre will provide the investigator with the allocation to receive either intervention A or B. The investigator will then obtain the appropriate intervention for the patient, which will be stored on the ICU.
Patients were randomised with balanced allocation to receive either SC placebo or sarilumab (100, 150 or 200 mg every other week (q2w), or 100 or 150 mg every week (qw), with q2w dosing alternating with placebo) for 12 weeks.
Patients mechanically ventilated for more than 7 days who are alert and able to co-operate with training (Riker Sedation Agitation Score 14 of 4) and can provide informed consent will be randomised (computer-generated random number sequence, concealed allocation) to receive either IMT or usual physiotherapy care.
The women were randomised using a computer-generated random number allocation to receive either four cycles of docetaxel (100 mg/m), followed by four cycles of combined fluorouracil (500 mg/m), epirubicin (10 0 mg/m) and cyclophosphamide (500 mg/m) (FEC100) (Arm 1), or the reverse order of drugs (FEC100 followed by docetaxel) (Arm 2).
Sixty health services (40 general practices and 20 Aboriginal Community Controlled Health Services (ACCHSs) will be randomised in a 1 1 allocation to receive either the intervention package or continue with usual care, stratified by service type, size and participation in existing quality improvement initiatives.
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The allocation to receive SDR is stamped on the data collection forms of each contact group.
In this pilot randomised controlled trial, 120 people with diabetes will be randomised with equal allocation to receive the intervention or usual clinical care.
Continued GP non-responders were randomised within their original allocation to receive a full or an abridged questionnaire reminder (see flowcharts 1 and 2 for full details).
Inclusion criteria: Patients with a clinical stage I endometrioid adenocarcinoma or complex atypical hyperplasia are randomized in a 2 1 allocation to receive TLH or TAH.
Although women and their care providers were not informed of swab results, those randomized to the treatment group were aware of the result because of their allocation to receive medication.
Women were randomised (randomisation procedure and allocation concealment not specified) to receive either a single pessary containing 150 mg chlorhexidine for two consecutive nights (n = 43), or a single 2 g oral dose of metronidazole (n = 36).
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