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A secondary goal was 50% improvement in GERD score and frequency of retreatment (patients in both groups with continuing symptoms after 3 months were eligible for Enteryx retreatment).
Methods Adult patients with a moderate-severe TBI (Glasgow Coma Scale 3 12) consecutively admitted to the intensive care unit (ICU) at a single trauma referral centre over 12 months were eligible following informed consent.
Subjects on stable testosterone replacement for ≥6 months were eligible.
HCWs who were providing ART services at least twice a week and had been working at the site for at least 12 months were eligible to participate.
Males age 15 to 25 years who had HBV surface antigen (HBsAg) present in blood for over 6 months were eligible.
Videos from workshops held in the past 12 months were eligible, as well as individual entries.
Patients whose active disease was stable for over 2 months were eligible for this study.
Only patients under maintenance PD for more than 3 months were eligible in the current study.
Children residing in the study area for at least six months were eligible for the study.
Patients with platinum-resistant (PFI <6 months) or platinum-sensitive disease (PFI ≥ 6 months) were eligible.
Patients with brain metastases that were controlled for >3 months were eligible.
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