Sentence examples for and explain the trial from inspiring English sources

At the beginning of the trial, in-hospital meetings were organized with members of the scientific committee, ED and ICU staff to introduce and explain the trial.

A KMD will thoroughly examine all inclusion/exclusion criteria and explain the trial to eligible patients.

The treating surgeon or a member of the study staff will introduce and explain the trial to the patient and address any questions the patient might have.

Patients who are interested in trial participation will be invited by the interface clinician to see a Research Nurse, who will further confirm eligibility and explain the trial in full.

Before vaccination related activities are initiated, local social mobilisation experts visit the residents of the main ring site around the index patient's residence, seek their consent for the trial team to approach them, through community leaders and representatives where applicable, and explain the trial's objectives and the implications of potential participation.

Patients' history and standard neurological examination will be documented by the neurosurgeon, who subsequently decides on the eligibility of the patient for the trial, based on Table 1, and explains the trial to the patient.

A leaflet and covering letter will explain the trial purpose and design, making it clear that women will only become eligible for the study if they require an instrumental delivery.

NERS coordinators in each area undertook briefings with primary care teams to explain the trial and to provide referral forms and trial information materials.

The research nurse will ask eligible women to participate, explain the trial and obtain informed consent, collect baseline data and ask women to self-collect a vaginal swab.

The research midwife will explain the trial and obtain informed consent, collect baseline data and randomly allocate (using telephone randomisation) women to study or control groups.

A research nurse will ask eligible women to participate, explain the trial and obtain informed consent, collect baseline data and randomly allocate women (using telephone randomisation) to one of the study groups.