Overview

Assessment of Gastric pH Changes Induced by Ascorbic Acid Tablets

Status:
Not yet recruiting
Trial end date:
2022-12-15
Target enrollment:
0
Participant gender:
Male
Summary
This study evaluates the use of ascorbic acid, vitamin C, to temporary reduce gastric pH in individuals with omeprazole induced hypochlorhydia. All participants will receive ascorbic acid tablets to measure the change in gastric pH.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Indiana University
Collaborators:
Butler University
Hala Fadda
Treatments:
Ascorbic Acid
Omeprazole
Criteria
Inclusion Criteria:

- Healthy, young males age 18-30 years with no prior history of gastrointestinal disease
or symptoms.

Exclusion Criteria:

- Hypochlorhydria (baseline use antacids, antisecretory medications, or surface agents
including proton-pump inhibitors, H2 blockers, or sucralfate).

- Current or previous history of gastrointestinal disease including gastroesophageal
reflux disease, Barrett's esophagus, peptic ulcer disease, dyspepsia, gastroparesis,
bacterial overgrowth, microscopic colitis, gastric intestinal metaplasia or
metaplastic atrophic gastritis, gastric neuroendocrine tumors, helicobacter pylori
infection, inflammatory bowel disease (Crohn's disease or ulcerative colitis), celiac
disease, visceral cancer, chronic infectious disease, immunodeficiency, uncontrolled
thyroid disease, history of liver disease).

- History of gastric bypass or other abdominal surgeries excluding cholecystectomy or
appendectomy > 6 months prior to study initiation.

- Radiation therapy to the abdomen.

- Pregnant females.

- Ingestion of any prescription, over-the-counter, or herbal medications which may
affect study interpretation.

- Currently a smoker

- Antibiotic use within the last 3 months