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Completed

NCT Number: NCT01204515

Abdominal Symptom Phenotype Study in Children

Children and adults commonly suffer from recurrent abdominal (stomach) pain. One type is called irritable bowel syndrome (IBS). IBS in adults and children is one of the most common and costly health care problems in the US. Some children have pain frequently (recurrent pain) while others rarely have pain. The investigators are conducting this study to help us answer questions about the causes and treatments, and management of IBS in children.

The purpose of this study is to find out if there is more than one type of IBS in children. If there is, this will be important in deciding the best treatments. The investigators also want to learn how children with IBS differ from those who do not have recurrent abdominal (stomach) pain.

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Key information

About this study

Functional gastrointestinal (GI) disorders (FGIDs), in particular irritable bowel syndrome (IBS) in adults and children, are among the most common and costly health care problems in the US. IBS disproportionately affects adult women (10-15% in western nations) and adolescent girls. Yet, health care providers remain challenged to provide effective clinical management. The etiology of IBS is not well defined and likely multi-factorial.

A Need to Define Subgroups of IBS:

This study emerges from the claim that identification of patient subgroups will advance our understanding of IBS and ultimately help develop treatment approaches. Most studies have lumped together patients with IBS into 2 groups (constipation-, diarrhea-predominant) and tested whether they differ from healthy controls. We propose that a paradigm shift is in order. We should recognize that IBS likely has multiple causes and therefore, multiple expressions. We speculate that by understanding better defined patient subgroups and linking them to newer biomarkers or tests, ultimately will further the understanding of the origins and create effective treatments.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

IBS:

  • Age 7-12 years
  • Females
  • Meet criteria for irritable bowel syndrome without evidence of organic disease
  • Developmentally normal
  • English speaking (as the psychological measures are either not available or validated in Spanish)
  • No other chronic, significant (e.g., diabetes, migraines) medical conditions
  • No menses

Controls:

  • Age 7-12 years
  • Females
  • No abdominal pain
  • No GI or chronic medical conditions (e.g., diabetes)
  • Developmentally normal
  • English speaking (as the psychological measures are not available or validated in Spanish)
  • No menses

Exclusion criteria

  • Non-english speaking
  • Developmentally or cognitively impaired
  • Males
  • Menses
  • No mother in the household for administration of the psychological measures
  • Use of any anti-depressants
  • History of migraines or chronic pain disorders
  • On narcotics for at least 1 week prior to enrollment
  • On any NSAIDs or pain reliever for at least 24 hours prior to enrollment
  • Sought psychotherapy in past 6 months for abdominal pain

Treatment and study plan

Primary outcomes

  1. Compare biomarkers (tests) on girls with and without IBS

    Time frame: Two Days

    Biomarkers: Proteomic analysis of urine samples; Results of video capsule endoscopy (VCE) using the PillCam; Serum lymphocyte activation and cytokine levels (IL-8, IL-10 and IL-12) Responses to DNIC procedure;

  2. Compare the response of stress in girls with and without IBS

    Time frame: One Day

    Salivary cortisol levels prior to and after the diffuse noxious inhibitory control (DNIC) procedure; Psychological characteristics of the child and mother

Sponsors and collaborators

Lead sponsor

Baylor College of Medicine

Other

Collaborators

  • National Institute of Nursing Research (NINR)
  • University of Washington

Registry information

Official study title

Abdominal Symptom Phenotype: Pathways to New Biomarkers

Acronym: ASPPNB

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Sep 17, 2010
Registry last updated
Feb 6, 2013

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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