Safety of Lactobacillus Rhamnosus GG Vs. Placebo in Elderly Subjects Receiving Trivalent Inactivated Influenza Vaccine
Status: | Completed |
---|---|
Conditions: | Healthy Studies, Influenza |
Therapuetic Areas: | Immunology / Infectious Diseases, Other |
Healthy: | No |
Age Range: | 65 - 80 |
Updated: | 1/12/2017 |
Start Date: | September 2011 |
End Date: | May 2012 |
Double Blind Randomized Controlled Trial to Evaluate the Safety of Lactobacillus Rhamnosus GG ATCC 53103 (LGG) Vs. Placebo in Elderly Subjects Receiving Trivalent Inactivated Influenza Vaccine
This is a phase I, randomized controlled trial to evaluate the safety of Lactobacillus
rhamnosus GG (LGG) versus placebo in elderly subjects receiving the trivalent inactivated
influenza vaccine. Lactobacilli are part of the normal flora of the intestine. LGG is one of
several strains of Lactobacilli that is used as a probiotic or microorganism administered to
confer "health benefits". Our research is focused on studying the possible therapeutic
effects of LGG. The study hypotheses are:
1. LGG or placebo administered twice daily will be safe and well tolerated in elderly
subjects who have just received the trivalent inactivated influenza vaccine
2. The immune response to the influenza vaccine at day 21, 28, 56, and at the end of the
influenza season will be higher in the LGG group than the placebo group
3. The occurrence rate of influenza like illness during the influenza season will be lower
in the LGG group than in the placebo group
4. The diversity of the microbiota in nasopharyngeal and stool specimens at day 21, 28, 56
and at the end of the influenza season will be greater in the LGG group than the
placebo group.
rhamnosus GG (LGG) versus placebo in elderly subjects receiving the trivalent inactivated
influenza vaccine. Lactobacilli are part of the normal flora of the intestine. LGG is one of
several strains of Lactobacilli that is used as a probiotic or microorganism administered to
confer "health benefits". Our research is focused on studying the possible therapeutic
effects of LGG. The study hypotheses are:
1. LGG or placebo administered twice daily will be safe and well tolerated in elderly
subjects who have just received the trivalent inactivated influenza vaccine
2. The immune response to the influenza vaccine at day 21, 28, 56, and at the end of the
influenza season will be higher in the LGG group than the placebo group
3. The occurrence rate of influenza like illness during the influenza season will be lower
in the LGG group than in the placebo group
4. The diversity of the microbiota in nasopharyngeal and stool specimens at day 21, 28, 56
and at the end of the influenza season will be greater in the LGG group than the
placebo group.
Inclusion Criteria:
1. Age 65-80 years
2. Willing to complete the informed consent process
3. Able and willing to participate for the planned duration of the study, including
availability for follow-up telephone contact
4. Is community dwelling for the past two years
5. Has received routine physical in the past two years
6. Has no new chronic conditions in the past two years
7. Identifies a primary care clinician
8. Has received recommended preventive services (Task Force for Clinical Preventive
Services) for vaccination and cancer prevention/detection, e.g.:
1. Pneumococcal vaccination
2. Mammography
3. Screening colonoscopy for cancer
9. Willing to comply with protocol and report on compliance and side effects during the
study period
10. Informed consent obtained and signed prior to screening
Exclusion Criteria:
1. Self-reported vaccination with influenza vaccine for the current season
2. Vaccination with any vaccine within the one month period prior to study enrollment or
intent to receive any other vaccine during the study period
3. History of hypersensitivity to any influenza vaccine components including thimerosal
or egg
4. History of Guillain-Barre syndrome
5. History of avoidance of egg and/or egg based products for any reason
6. Acute febrile illness within the week prior to immunization - immunization deferred
until illness resolved
7. Consumption of supplements or food products containing LGG or probiotics for 28 days
prior to the start of the study or consumption of yogurt that has the "live and
active cultures" seal
8. Known or suspected allergies to probiotics, Lactobacillus, microcrystalline
cellulose, gelatin, or antibiotics that may be used to treat LGG bacteremia or
infection
9. Received oral or parenteral antibiotics within 4 weeks of enrollment or prescribed
antibiotics on the day of enrollment
10. Drug or alcohol abuse within the previous 12 months
11. Hospitalization, major surgery or endoscopy within the last 3 months
12. Scheduled hospital admission within 3 months of enrollment
13. Resident of a nursing home or rehabilitation center
14. Presence of any of the following:
1. Grade 2 or higher abnormal vital signs or abnormalities on physical exam
2. Indwelling catheter or implanted hardware/prosthetic device or feeding tube
3. Current or within the last 2 years, any episode of bowel leak, acute abdomen,
diverticulitis, bloody bowel movements or peptic ulcer disease, including any
surgical procedure or current prescription medications for any of these
conditions
4. Current or within the last 4 weeks, active bowel disease such as an episode of
infectious or non-infectious diarrhea, constipation or vomiting lasting more
than 12 hours or current prescription medications for any of these conditions
5. Any history of gastric or intestinal dysmotility, slowed transit time, variable
small intestinal permeability, pancreatitis, history of disease or current
prescription medication for any of these conditions
6. Any history of Hepatitis B or Hepatitis C infections, cirrhosis, or chronic
liver disease
7. Underlying structural heart disease such as abnormal native heart valve
replacement, Stage IV congestive heart failure
8. History of peripheral vascular disease or stroke
9. Immunosuppression including HIV positive, solid organ or stem cell transplant
recipient, receiving any oral or parenteral immunosuppressive therapy,
neutrophil count <500/mm^3, or an anticipated drop in the neutrophil count to
<500/mm^3 or active or planned chemotherapy or radiotherapy
10. History of collagen vascular or autoimmune disease
11. End stage renal disease
12. History of chronic obstructive pulmonary disease or asthma
13. Diabetes or thyroid disease
14. Active tuberculosis (TB), defined as undergoing a work up for suspected active
TB infection or currently on treatment for active TB
15. Positive drug or alcohol testing at screening or positive breathalyzer at baseline or
an unwillingness to undergo drug and alcohol testing
16. Abnormal laboratory tests defined as any of the following:
1. White blood cell (WBC) <3.3 or > 12.0 K/microliter
2. Platelets < 125 K/microliter
3. Hemoglobin Males: < 12.0 g/dL; Females < 11.0 g/dL
4. Creatinine > 1.8 mg/dL
5. Blood Urea Nitrogen (BUN)> 27 mg/dL
6. Aspartate aminotransferase (AST) > 1.25 ULN
7. Alanine aminotransferase > 1.25 ULN
8. Alkaline phosphatase > 2.0 ULN
9. Bilirubin (total) > 1.5 ULN
10. Glucose (nonfasting) > 126 mg/dL
11. Positive HIV, Hepatitis B surface antigen or Hepatitis C antibody
17. Any other condition that in the opinion of the investigator would jeopardize the
safety or rights of the subject participating in the study or would make it unlikely
the subject could complete the study
We found this trial at
1
site
Click here to add this to my saved trials