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In addition, at each investigators meeting, these guidelines were systematically discussed to reinforce compliance.
We reviewed and discussed the behavioural interventions at each investigators' meeting.
Ethical approval was obtained by Institutional Review Boards at each investigators site.
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Adverse events are classified by each investigator using three criteria in specific order: seriousness, expectedness and relatedness to the investigational intervention.
Each investigator involved in the search for the letter was offered antibiotics.
An increasing share of drugs are tested at multiple sites, with each investigator having only a limited number of subjects.
Anesthesia was at the discretion of each investigator.
Three sonographic measurements were made by each investigator on each tendon.
Consensus meeting dealt the cases with any difficulty in diagnosis by each investigator.
Each investigator center will submit the study protocol to its Institutional Review Board IRBB).
A standardized questionnaire was completed by each investigator at the time of the clinical evaluation.
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