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Completed

NCT Number: NCT01972334

Stool Transplant in Pediatric Patients With Recurring C. Difficile Infection

The incidence of C. difficile infection (CDI) has alarmingly increased over the past several years and the affected population has expanded to include those previously at low risk, such as children. The annual US financial burden associated with this infection is great and estimated to exceed $1.8 billion. C. difficile infection arises when the gut microbial ecology is disrupted during interventions notorious for perturbing the delicate microbial balance. A well known and common example is the use of antibiotics. Fecal microbiota transplant (FMT) has been introduced several decades ago in an attempt to restore the gut microbial balance. To this date there have been a great number of reports of success in eliminating recurrent C. difficile infections and restoring the gut microbial profile to resemble that of the healthy donor. While over 300 cases have been described in the literature, there has been no pediatric controlled studies performed to compare its efficacy to placebo. Therefore, there is a strong need to determine their safety and efficacy in pediatric randomized controlled studies. The investigators hypothesize that children with recurrent C. difficile infection will respond to fecal transplant therapy which will modify their gut microbial profile. The investigators propose a randomized, placebo controlled, pilot study of fecal microbial transplant in children with recurrent C. difficile infection to evaluate the safety and efficacy of fecal microbial transplant in children in preventing recurrent C. difficile infection. The investigators anticipate that fecal microbial transplant in children with recurrent C. difficile infection will be safe and efficacious and will provide these children with a great alternative to a disease that is difficult to treat. Results of this study will establish the major role of the gut microbiome in this disease and demonstrate the viability of gut microbial transplant in recipients.

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Key information

Age range

1 year–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Miller Children's Hospital

Los Angeles, California, 90806, United States

About this study

Forty six children with recurrent C. difficle infection will be randomized 1:1 to receive either fecal microbial transplant or placebo. The safety and efficacy of this intervention will be monitored for one year.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 1-21.
  • Recurrent C. difficile infection defined as the occurrence of more than two infections

Exclusion criteria

  • Inflammatory bowel disease
  • Immune-deficiency.
  • Allergy to oral vancomycin.
  • Children colonized with Clostridium difficile without evidence of symptoms to suggest colitis such as diarrhea and/or rectal bleeding.
  • Concurrent infections that require anti-microbial therapy.
  • Unable to give informed consent/assent.
  • Pregnancy.

Treatment and study plan

FMT

Biological

as explained in study arm

Other names: fecal microbial transplant, stool transplant

Placebo

Biological

salt water or saline will be given as placebo

Other names: saline, salt water

Primary outcomes

  1. The primary efficacy outcome of this randomized, controlled, double-blinded study is the time of recurrence of an infection

    Time frame: 12 months

    secondary outcome measures are focused on the safety of Fecal microbial transplant in this population and all subjects will be closely monitored for developing adverse events for 12 months

Secondary outcomes

  1. safety of fecal microbial transplant in children with recurrent clostridium difficile

    Time frame: 12 months

    All subjects will be closely monitored for adverse events for 12 months after fecal transplant. Subjects will be asked to report any adverse events as they occur and will also be monitored during each visits especially fever, bloating, abdominal pain, vomiting, diarrhea, and rectal bleeding.

Sponsors and collaborators

Lead sponsor

MemorialCare Health System

Other

Collaborators

  • Memorial Medical Center Foundation

Registry information

Official study title

A Randomized, Placebo-controlled Pilot Trial to Administer Fecal Microbial Therapy (Stool Transplant) or Placebo in Children Ages 8 to 18 With Recurrent C. Difficile Infection

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Oct 30, 2013
Registry last updated
Sep 1, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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