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Patients will be requested to report any adverse events.
No informed consensus will be requested to patients [ 7].
They will be requested to continue their usual care.
Consent will be requested to continue to use routinely collected data for study purposes.
Those interested will be requested to come to the antenatal clinic for recruitment and randomisation.
Consent will be requested to feedback clinical information back to the GP.
Those interested will be requested to come to the antenatal clinic for randomisation and recruitment.
Next you will be requested to fill the Vehicle information.
Patients will also be requested to consent to be contacted in the future.
will be requested from the user.
Further examinations will be requested as required.
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