Assessing Outcomes After Surgery for Gastroesophageal Reflux Disorder
Not Applicable
- Conditions
- Gastroesophageal Reflux Disorder
- Interventions
- Other: Symptom questionnaire
- Registration Number
- NCT00518505
- Lead Sponsor
- University of South Florida
- Brief Summary
The purpose of this study is to review pre-operative studies and patient evaluation reports and compare those with the results of the post-operative studies, patient evaluation reports and subjective patients' outcomes following laparoscopic surgery for gastroesophageal reflux disorder. This will allow us to evaluate how patients have benefited from the procedure.
- Detailed Description
This study will include all patients who have laparoscopic surgery for gastroesophageal reflux disorder. Patients who participate will be asked to answer questionnaires regarding symptoms of reflux before and after surgery. In addition medical charts will be reviewed for relevant data.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 1500
Inclusion Criteria
- patients must have GERD and must plan to have laparoscopic surgery for GERD.
- patients must be at least 18 years of age
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description I Symptom questionnaire This is a single arm study. All patients will be asked to complete questionnaires and have their medical charts reviewed.
- Primary Outcome Measures
Name Time Method The objective of this study is to review pre-operative studies and evaluation reports and compare those with post-operative studies and evaluation reports to evaluate outcome following laparoscopic surgery for GERD. 5 years
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Tampa General Hospital/University of South Florida
🇺🇸Tampa, Florida, United States