Canadian, multi-centre study of symptom burden and clinical management in subjects with GERD - RANGE

Inclusion Criteria

• - Provision of informed consent
• - Ability to complete PRO instruments (non-applicable to "non-attendees")
• - Subject with GERD symptom(s). At least presence of troublesome heartburn and/or regurgitation even if not specifically recorded at the Index Visit.
• - At least one visit during the Retrospective Visit Period (-6 to -2 months prior to study start).
• In the reasons for the Index Visit section of the medical record mention of acid regurgitation and/or heartburn symptom(s) or GERD diagnosis or GERD complications has to be explicit or a treatment decision (prescription) in a previously diagnosed subject although no mention of symptoms is made.