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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00998244
Other study ID # 07-0623
Secondary ID
Status Completed
Phase N/A
First received October 2, 2009
Last updated January 6, 2012
Start date September 2009
Est. completion date December 2011

Study information

Verified date January 2012
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this research study is to learn if a very low carbohydrate (sugar) diet or traditional low fat diet is able to reduce symptoms related to gastroesophageal reflux disease (GERD) in people who are overweight. Patients with GERD may experience all or some of the following symptoms: stomach acid or partially digested food re-entering the esophagus (which is sometimes referred to as heartburn or regurgitation) and belching. In this study, the investigators also hope to find out if acid in the esophagus is reduced more by a low carbohydrate diet than a low fat diet.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- 18 to 70 years old

- BMI between 30 kg/m2 and 45 kg/m2

Exclusion Criteria:

- Known history of Barrett's esophagus or esophageal adenocarcinoma

- Previous surgical anti-reflux procedure

- Previous weight loss surgery, including gastric bypass

- Diabetes

- Pregnancy

- Heart Disease

- Unwillingness to discontinue use of proton pump inhibitors (PPI's) or H2-receptor antagonists per study protocol

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Other:
Diet - very low carb or low fat
Diet comparison in Gastroesophageal Reflux Disease

Locations

Country Name City State
United States The University of North Carolina at Chapel Hill Chapel Hill North Carolina

Sponsors (2)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill Takeda Pharmaceuticals North America, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in distal esophageal acid exposure after initiating a very low carbohydrate diet compared to the decrease seen after initiating a low fat diet Baseline, 10 days after baseline, and at 25 days after baseline. No
Secondary The change in serum levels of pro-inflammatory cytokines after initiating a very low carbohydrate diet compared to a traditional low fat diet as measured with blood samples. Baseline, 10 days after baseline, and at 25 days after baseline No
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