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Trial record 20 of 1404 for:    Peru

Safety of Lactobacillus Reuteri in Healthy Children Aged 2-24 Months (PRIDEC Peru)

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ClinicalTrials.gov Identifier: NCT02460575
Recruitment Status : Recruiting
First Posted : June 2, 2015
Last Update Posted : September 10, 2019
Sponsor:
Collaborators:
Johns Hopkins Bloomberg School of Public Health
Asociación Benéfica Prisma
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Information provided by (Responsible Party):
Richard A. Oberhelman, Tulane University School of Medicine

Brief Summary:
Phase I double blinded randomized trial of the safety and tolerability of Lactobacillus reuteri DSM 17938 given for five successive days in healthy children. Sixty children will receive study product at a treatment to placebo ratio of 2:1 and followed for 3 months for safety outcomes.

Condition or disease Intervention/treatment Phase
Healthy Biological: Lactobacillus reuteri 17938 Biological: Placebo Phase 1

Detailed Description:

The study is a single center Phase 1 double blind placebo controlled trial of Lactobacillus reuteri DSM 17938 in children aged 2-24 months. The study population is based in a community with a registered clinical trial center in rural Peru where this protocol can be done in a highly controlled setting. The study is intended to enroll healthy children living in a resource constrained setting where chronic undernutrition and diarrheal disease is common, as this is the population that is most likely to receive benefit from the use of this and or other probiotic products for the treatment of acute infectious diarrhea and environmental enteropathy.

Up to 100 subjects will be enrolled in order to obtain the randomization of 60 subjects, who will receive study product or placebo at a ratio of 2:1. Participants will be enrolled between the ages of 8 weeks and 24 months. There will be no age stratification. Participants will be screened with a baseline history and physical examination and laboratory tests to determine the HIV status of the child, as well baseline laboratory tests to evaluate occult infections, hepatic function, and renal function. Upon randomization subjects will be screened and randomized to a treatment arm. Product will be administered under the direct supervision of study staff daily for 5 days. The primary outcome is the safety and tolerability of the product at this dose and formulation. Safety will be assessed by the monitoring of baseline laboratory tests at 5 and 28 days following the initiation of therapy and by AE monitoring. Tolerability will be evaluated by analyzing 28 day diary cards that are distributed to all randomized subjects on which parents record their child's symptoms (specifically fever, anorexia/oral intake, vomiting, diarrhea, irritability, rash, wheezing, or open fields which allows them to describe any issue their child may experience and grade its severity) . Secondary outcomes include:

1) The assessment of the duration of shedding of Lactobacillus reuteri (Lr) strain DSM 17938 following administration. This will be determined by and endpoint PCR assay for L. reuteri done on stool collected on D3, D5, D12, D15, D18, D24, D28, D36 on all participants.

The planned enrollment period is four months and the participation of individual subjects is for 3 months. The study should be completed in 7 months. Safety monitoring by treatment group, i.e., infants assigned to active or placebo study product will be conducted by NIDDK appointed DSMB under the direction of the NIDDK Program Official.


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: L. Reuteri for Pediatric Diarrhea in Peru: Growth, Enteropathy, and Microbiota
Actual Study Start Date : January 9, 2019
Estimated Primary Completion Date : December 20, 2019
Estimated Study Completion Date : March 1, 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Lactobacillus
Active Product: Description Lactobacillus reuteri 17938 suspended in sunflower oil, medium chain triglyceride oil, silicone dioxide. Total viable count of L. reuteri 17938 1 x 108 CFU/5 drops.
Biological: Lactobacillus reuteri 17938
probiotic

Placebo Comparator: Placebo
Composition Sunflower oil, medium chain triglyceride oil and silicon dioxide. Total viable count of L. reuteri is zero CFU/ 5 drops.
Biological: Placebo
Composition Sunflower oil, medium chain triglyceride oil and silicon dioxide. Total viable count of L. reuteri is zero CFU/ 5 drops.




Primary Outcome Measures :
  1. number of participants with positive blood culture for L. reuteri [ Time Frame: Participants are followed for an average of 36 days ]
  2. Mean daily temperature [ Time Frame: 5 days of study product administration ]


Information from the National Library of Medicine

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Ages Eligible for Study:   2 Months to 24 Months   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • In order to be eligible to participate in this study, a subject must meet all of the following criteria:

    • Have a parental permission form signed by both parents
    • Be between 8 weeks to 24 months of age with no preexisting exclusion criteria
    • Have parents who are willing to comply with all planned study procedures and be available for planned study visits for 3 months.

Exclusion Criteria:

  • 1) No enrollment of family members in households where any of the following are present:

    1. Another study participant in the household
    2. Presence of immune suppressed individuals or use of immunosuppressive agents (including but not limited to corticosteroids, methotrexate, etc.) by any household member
    3. Presence of a serious congenital anomaly or chronic medical condition that in the opinion of the investigators would contraindicate participation in any household member, including history of gastrointestinal surgery, chronic gastrointestinal illness, abnormal intestinal anatomy, or abnormal bowel functionality

      The following risk factors are at the level of the individual child:

      2) Allergy to penicillin, cephalosporins, clindamycin or gentamicin 3) History of antibiotic use in the last 30 days 4) Use of probiotic products within the past 30 days, including masato (local product with fermenting bacteria) and yogurt products containing live bacterial cultures.

      5) History of diarrheal illness within the past 30 days (See definition in Protocol Appendix B) 6) Presence of fever or a pre-existing adverse event monitored in the study (See Protocol Appendix B Definitions of AEs for specific adverse events monitored in the study) 7) Positive results on serum diagnostic tests for antibodies to HIV.

      8) Presence of severe anemia, defined as serum hemoglobin < 7 gm/dL

      9) Out of range laboratory values for total leucocyte count, BUN, Creatinine, AST, ALT, and total bilirubin monitored as potential adverse events, as described in Appendix E.

      10) Pre-enrollment stool sample (collected within 14 days of day 1 of the study) is positive for L. reuteri by PCR.


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02460575


Contacts
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Contact: Margaret N Kosek, MD (410)-955-5932 mkosek@jhmi.edu
Contact: Pablo Yori, MS (443) 900-7270 pyori@jhu.edu

Locations
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Peru
Centro de Salud de Santa Clara Recruiting
Santa Clara, Loreto, Peru
Contact: Maribel Paredes, BS, MPH    011-5165-234250    mparedeso@prisma.org.pe   
Sponsors and Collaborators
Tulane University School of Medicine
Johns Hopkins Bloomberg School of Public Health
Asociación Benéfica Prisma
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Investigators
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Principal Investigator: Margaret N Kosek, MD Johns Hopkins Bloomberg School of Public Health

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Responsible Party: Richard A. Oberhelman, Professor, Tulane University School of Medicine
ClinicalTrials.gov Identifier: NCT02460575     History of Changes
Other Study ID Numbers: U01DK105849 ( U.S. NIH Grant/Contract )
U01DK105849 ( U.S. NIH Grant/Contract )
First Posted: June 2, 2015    Key Record Dates
Last Update Posted: September 10, 2019
Last Verified: September 2019

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Richard A. Oberhelman, Tulane University School of Medicine:
Safety