ClinicalTrials.gov
ClinicalTrials.gov Menu

Assessing Outcomes After Surgery for Gastroesophageal Reflux Disorder (GERD)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00518505
Recruitment Status : Unknown
Verified August 2012 by Kenneth Luberice, University of South Florida.
Recruitment status was:  Recruiting
First Posted : August 20, 2007
Last Update Posted : August 15, 2012
Sponsor:
Information provided by (Responsible Party):
Kenneth Luberice, University of South Florida

August 16, 2007
August 20, 2007
August 15, 2012
December 2006
September 2017   (Final data collection date for primary outcome measure)
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. [ Time Frame: 5 years ]
  • 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. [ Time Frame: 5 years ]
  • The objective of this study is to review pre-operative studies and patient evaluation reports and compare those with post-operative studies and patient evaluation reports to evaluate outcome after laparoscopic surgery for GERD [ Time Frame: 5 years ]
Complete list of historical versions of study NCT00518505 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Assessing Outcomes After Surgery for Gastroesophageal Reflux Disorder
Long and Short Term Outcomes After Laparoscopic Surgery for Gastroesophageal Reflux Disease
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.
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.
Interventional
Not Applicable
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Gastroesophageal Reflux Disorder
Other: Symptom questionnaire
This questionnaire will assess patient outcomes before and after surgery for gastroesophageal reflux disorder.
I
This is a single arm study. All patients will be asked to complete questionnaires and have their medical charts reviewed.
Intervention: Other: Symptom questionnaire
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
1500
Same as current
September 2017
September 2017   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • patients must have GERD and must plan to have laparoscopic surgery for GERD.
  • patients must be at least 18 years of age
Sexes Eligible for Study: All
18 Years and older   (Adult, Older Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00518505
105238
No
Not Provided
Not Provided
Kenneth Luberice, University of South Florida
University of South Florida
Not Provided
Study Director: Alexander S Rosemurgy, M.D. University of South Florida
University of South Florida
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP