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Early Phase 1 N=12 Treatment

Role of Methane in Glycemic Control

Diabetes · Obesity

Enrolled (actual)
12
Serious AEs
0.0%
Results posted
May 2019
Primary outcome: Primary: Number of Subjects Who Eradicated Methane on Breath Test — 8 participants

Study Design & Population

Study type
Interventional
Phase
Early Phase 1
Interventions
Neomycin (Drug); Rifaximin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Cedars-Sinai Medical Center
Primary completion
Apr 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects Who Eradicated Methane on Breath Test
8
PRIMARY
Stool Methanogen Levels
3.6*10^7; 6.86*10^8; 1.1*10^5; 9.4*10^7 0.16
PRIMARY
Stool Total Bacteria Levels
1.1*10^9; 3.7*10^8; 1.2*10^9; 8.5*10^9
PRIMARY
Low Density Lipoprotein (LDL) Levels Before and After Antibiotic Therapy
116; 96; 104; 111 0.028 sig
PRIMARY
Total Cholesterol Levels Before and After Antibiotic Therapy
192; 173; 177; 188 0.01 sig
PRIMARY
Average Daily Caloric Loss in Stool
8.1; 8.3; 8.3; 8.3 0.97
PRIMARY
Gastric Emptying
182.3; 174.9; 163.5; 164.9 0.61
SECONDARY
Bowel Symptoms - Bloating
55.09; 66.8; 39.91; 38.9 0.018 sig
SECONDARY
Bowel Symptoms - Abdominal Pain
23.36; 28.6; 18.18; 21.6 0.43
SECONDARY
Bowel Symptoms - Constipation
30.18; 31.0; 20.55; 22.3 0.13
SECONDARY
Bowel Symptoms - Diarrhea
23.73; 30.5; 14.64; 17.3 0.29
SECONDARY
Bowel Symptoms - Straining
31.64; 37.5; 21.55; 18.4 0.22
SECONDARY
% Stool Dry Weight
24.1; 25.1; 22.9; 22.6 0.33

Summary

The purpose of this study is to determine how certain types of bacteria in the human gut may affect weight gain, and contribute to the development of diabetes. The investigators initial studies have shown that gut bacteria that produce methane may directly affect weight gain. These bacteria, called methanogens, produce methane gas as a byproduct, which can be detected through breath testing. Methane can slow the passage of food through the intestines, which would allow extra time for uptake and absorption of nutrients and calories, and might contribute to weight gain. The investigators have also found that people who have increased levels of methane-producing bacteria in their intestines also have higher levels of glucose in their blood. Therefore, control of how the body responds to insulin and uses glucose may be altered in methane-producing individuals. This research study is designed to test the investigational use of the drugs neomycin and rifaximin that have been approved by the U.S Food and Drug Administration (FDA). While neomycin is FDA-approved for treating skin infections, preparing the bowel for surgery, and hepatic encephalopathy (a condition that occurs when a damaged liver cannot remove the toxins that a healthy liver normally would), and rifaximin is FDA-approved for treating travelers' diarrhea, they are not yet approved to be used together for the treatment of methanogens or obesity.

Eligibility Criteria

Inclusion Criteria

  • 18-65 years old with pre-diabetes (hemoglobin a1c of 5.7-6.4%)
  • BMI > 25.0
  • presence of methane on a breath sample (>3ppm)

Exclusion Criteria

Subjects will be excluded from the study if they exhibit any of the following:

  • Diabetes/diabetes medications
  • Prokinetic medication
  • Pregnancy
  • History of bariatric or intestinal surgery (other than cholecystectomy or appendectomy)
  • Unstable thyroid disease
  • An active weight loss treatment/plan
  • Smoking
  • Dietary restrictions (lactose intolerance, vegan etc)
  • Other inability to comply with the study procedures, including known allergy to the study antibiotics (neomycin and rifaximin)
  • Active inflammatory bowel disease (celiac, Crohn's disease, ulcerative colitis)
  • Antibiotic use in the past month
  • Subjects who do not have a microwave (for reheating study meals) and a freezer (for storing leftovers and stool samples) will be excluded from this study.
  • Subjects who have an aspirin sensitivity
  • Proton pump inhibitor medications or antacids
  • History of bezoar
  • Disorders of swallowing
  • Suspected strictures, fistulas or physiological GI obstruction
  • GI surgery within 3 months
  • Severe dysphagia to food or pills
  • Diverticulitis
  • Subjects who use an implanted or portable electromechanical device such as a cardiac pacemaker or infusion pump
  • Subject who have a peanut allergy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01638429). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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