Obesity Clinical Trial
Official title:
Methane Production and Glycemic Regulation in Pre-diabetic Subjects: Role of Methane in Glycemic Control
| NCT number | NCT01638429 |
| Other study ID # | 25182 |
| Secondary ID | |
| Status | Completed |
| Phase | Early Phase 1 |
| First received | |
| Last updated | |
| Start date | April 2012 |
| Est. completion date | April 2014 |
| Verified date | January 2019 |
| Source | Cedars-Sinai Medical Center |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
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.
| Status | Completed |
| Enrollment | 11 |
| Est. completion date | April 2014 |
| Est. primary completion date | April 2014 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 65 Years |
| Eligibility |
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 |
| Country | Name | City | State |
|---|---|---|---|
| United States | Cedars-Sinai Medical Center | Los Angeles | California |
| Lead Sponsor | Collaborator |
|---|---|
| Cedars-Sinai Medical Center | American Diabetes Association |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Number of Subjects Who Eradicated Methane on Breath Test | Number of subjects who exhibited a decrease in breath methane levels to below detectable (below 3ppm) following antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment breath tests were performed within 2 weeks (14 days) of completing the course of antibiotics. |
Baseline and 1-14 days following completion of antibiotic treatment | |
| Primary | Stool Methanogen Levels | Stool methanogen levels were measured in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment stool samples were collected within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Methane Eradicators (subjects who eradicated methane on breath test following antibiotic treatment) (N=8) Group 2 - Methane Non-eradicators (subjects who did not eradicate methane on breath test following antibiotic treatment) (N=3) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Primary | Stool Total Bacteria Levels | Stool total bacteria levels were measured in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics.Post-treatment stool samples were collected within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Methane Eradicators (subjects who eradicated methane on breath test following antibiotic treatment) (N=8) Group 2 - Methane Non-eradicators (subjects who did not eradicate methane on breath test following antibiotic treatment) (N=3) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Primary | Low Density Lipoprotein (LDL) Levels Before and After Antibiotic Therapy | LDL levels were measured in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment blood samples were collected within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Methane Eradicators (subjects who eradicated methane on breath test following antibiotic treatment) (N=8) Group 2 - Methane Non-eradicators (subjects who did not eradicate methane on breath test following antibiotic treatment) (N=3) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Primary | Total Cholesterol Levels Before and After Antibiotic Therapy | Total cholesterol levels were measured in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics.Post-treatment blood samples were collected within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Methane Eradicators (subjects who eradicated methane on breath test following antibiotic treatment) (N=8) Group 2 - Methane Non-eradicators (subjects who did not eradicate methane on breath test following antibiotic treatment) (N=3) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Primary | Average Daily Caloric Loss in Stool | The daily caloric loss in stool for each subject was calculated by expressing the total number of kcalories lost in stool over a 3-day period as a percentage of the total number of kcalories ingested over the same 3 days (the number of calories ingested = the number available in meals provided less the number remaining in leftovers). Caloric content for meals, leftovers, and stool was determined by bomb calorimetry. This average daily caloric loss for each group was then compared before and after antibiotic therapy. Post-treatment caloric harvest studies were performed within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Primary | Gastric Emptying | Gastric Emptying times (minutes) were determined in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment gastric emptying studies were performed within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | Bowel Symptoms - Bloating | Bowel symptom scores on a visual analog scale (VAS) were compared in all subjects before and after antibiotic treatment. Scale values were from 0 to 100, where 0 indicates no symptom and 100 indicates severe symptoms. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment symptom scores were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | Bowel Symptoms - Abdominal Pain | Bowel symptom scores on a visual analog scale (VAS) were compared in all subjects before and after antibiotic treatment. Scale values were from 0 to 100, where 0 indicates no symptom and 100 indicates severe symptoms. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment symptom scores were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | Bowel Symptoms - Constipation | Bowel symptom scores on a visual analog scale (VAS) were compared in all subjects before and after antibiotic treatment. Scale values were from 0 to 100, where 0 indicates no symptom and 100 indicates severe symptoms. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment symptom scores were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | Bowel Symptoms - Diarrhea | Bowel symptom scores on a visual analog scale (VAS) were compared in all subjects before and after antibiotic treatment. Scale values were from 0 to 100, where 0 indicates no symptom and 100 indicates severe symptoms. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment symptom scores were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | Bowel Symptoms - Straining | Bowel symptom scores on a visual analog scale (VAS) were compared in all subjects before and after antibiotic treatment. Scale values were from 0 to 100, where 0 indicates no symptom and 100 indicates severe symptoms. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment symptom scores were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) |
Baseline and 1-60 days following completion of antibiotic treatment | |
| Secondary | % Stool Dry Weight | % stool dry weight [total stool dry weight (g)/total stool fresh weight (g)] was determined in all subjects before and after antibiotic treatment. After baseline (pre-treatment) testing, subjects underwent a 10-day course of antibiotics. Post-treatment stool samples were obtained within 31 days (1 month) of completing the course of antibiotics. One subject received an exemption from this requirement and completed testing within 60 days. For analysis, subjects were grouped into two groups: Group 1 - Total study population (methane eradicators and non-eradicators, N=11) Group 2 - Methane eradicators (subjects who eradicated methane on breath test following antibiotic treatment, N=8) | Baseline and 1-60 days following completion of antibiotic treatment |
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