Safety of Lactobacillus Rhamnosus GG Vs. Placebo in Elderly Subjects Receiving Trivalent Inactivated Influenza Vaccine

Healthy Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01368029
• Other study ID #: 2010 P 001694
• Status: Completed
• Phase: Phase 1
• First received: June 2, 2011
• Last updated: January 10, 2017
• Start date: September 2011
• Est. completion date: May 2012

Study information

• Verified date: January 2017
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: May 2012
• Est. primary completion date: May 2012
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 65 Years to 80 Years

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention

Related Conditions & MeSH terms

• Elderly
• Healthy
• Influenza, Human

Intervention

Biological:
• Lactobacillus rhamnosus GG ATCC 53103 (LGG)
Study drug capsules (1x10^10 LGG/capsule) are to be taken orally twice a day every day on an outpatient basis for 28 days
• Placebo
Placebo capsules composed of microcrystalline cellulose are to be taken orally twice a day on an outpatient basis for 28 days.

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Massachusetts General Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Occurrence of adverse events that are possibly or probably related to administration of LGG	Adverse events will be detected during study visits with standardized questionnaires, medical history, vital signs, physical examinations, laboratory tests and review of subject diaries as well as between study visits on telephone calls based on responses to adverse event questionnaires. Additionally, subjects are encouraged to call the PI or study staff at any time if they are experiencing an adverse event.	Subjects will be followed from the study start through the end of the influenza season (as defined by CDC) with an anticipated average for most subjects of 7 months.	Yes
Secondary	Anti-influenza systemic immune response	HAI, MN titers and IgA titers will be measured at days 21, 28, 56 and the end of the influenza season	Subjects will be followed from the study start through the end of the influenza season (as defined by CDC) with an anticipated average for most subjects of 7 months.	No
Secondary	Anti-influenza mucosal immune response	IgA titers will be measured at days 21, 28, 56 and at the end of the influenza season	Subjects will be followed from the study start through the end of the influenza season (as defined by CDC) with an anticipated average for most subjects of 7 months.	No
Secondary	Occurrence of influenza like illness	Influenza like illness is defined as a reported oral temperature of 100 degrees Fahrenheit with at least 2 symptoms of acute respiratory illness	Subjects will be followed from the study start through the end of the influenza season (as defined by CDC) with an anticipated average for most subjects of 7 months.	No
Secondary	Changes in the richness and bacterial diversity of the nasopharyngeal and gut microbiota and presence of LGG in stool specimens by routine culture	Stool and nasopharyngeal specimens will be analyzed to learn what bacteria are present during different phases of the study and how the types and quantities of bacteria may change over time	Subjects will be followed from the study start through the end of the influenza season (as defined by CDC) with an anticipated average for most subjects of 7 months.	No