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Secretin for the Treatment of Autism

Primary Purpose

Autism

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
secretin, synthetic porcine
secretin, biologically derived porcine
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autism focused on measuring Pervasive Developmental Disorders, Secretin, synthetic porcine, Secretin, biological porcine, Autism Diagnostic Observation Schedule - Generic (ADOS-G), Rimland Questionnaire, Expressive Vocabulary Test, MacArthur Communication Inventory, Aberrant Behavior Checklist

Eligibility Criteria

3 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria Autism based on DSM-IV criteria IQ > 35 Medically fit for the study in the judgment of the study officials Exclusion Criteria Prior administration of secretin Acute or chronic pancreatitis Use of anticholinergics within 72 hours of study entry or anticipated need for anticholinergics during study Allergies to pork products Use of investigational drug within 1 month of study entry Change in any medication or other therapeutic modality being used to treat any neurodevelopmental or gastrointestinal symptoms of the underlying autism disorder within 1 month of study entry Any medical condition which, in the judgment of the investigator, would make the patient unable to safely participate in the study or comply with all study procedures Any medical diagnosis which could account for autistic spectrum disorder (i.e., Rett syndrome, Fragile X, tuberous sclerosis, disintegrative disorder, epilepsy, Landau Kleffner, other mental retardation syndromes, or history of severe motor delays or current sensory or motor impairment such as cerebral palsy) Hearing or visual impairments Use of psychotropic medications (except for occasional symptomatic use for sleep, etc.) within 6 months of study entry

Sites / Locations

  • Children's Hospital
  • Center on Human Development and Disability

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
August 1, 2003
Last Updated
June 23, 2005
Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)
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1. Study Identification

Unique Protocol Identification Number
NCT00065962
Brief Title
Secretin for the Treatment of Autism
Official Title
Multisite Controlled Secretin Trial in Autism
Study Type
Interventional

2. Study Status

Record Verification Date
June 2003
Overall Recruitment Status
Completed
Study Start Date
June 1999 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2000 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborators
National Institute on Deafness and Other Communication Disorders (NIDCD)

4. Oversight

5. Study Description

Brief Summary
Many drugs used to treat autism target specific symptoms, such as hyperactivity and aggressiveness. Few drugs target the core autistic symptoms of impaired social interaction and communication. This study will evaluate two forms of the drug secretin for the treatment of core autistic symptoms.
Detailed Description
Autism is a disorder characterized by impairments of social interactions, verbal and nonverbal communication, and preoccupation with unusual activities or interests, particularly stereotyped or repetitive movements. This debilitating disorder is estimated to occur in 2 to 10 of every 10,000 births. A primary focus in pyschopharmacological intervention has been to treat specific associated symptoms, such as hyperactivity, aggressiveness, and temper tantrums; there are few pharmacologic treatments directed toward core autistic symptoms. Secretin is a gut hormone with binding sites in the brain. Previous research has described three patients with autism who underwent diagnostic endoscopy for gastrointestinal complaints and experienced dramatic improvement in autistic symptoms following the administration of intravenous secretin given as part of endoscopy. Though the results of this single, uncontrolled study have limited interpretive value, many autistic children have been exposed and continue to be exposed to this potential treatment in an uncontrolled manner. This double blind, placebo-controlled trial will evaluate the safety and efficacy of secretin for the treatment of autism. Participants will be randomly assigned to one of three treatment groups: synthetic porcine secretin (sPS), biologically derived porcine secretin (bPS), or placebo. Each participant will be given an initial intravenous dose of 0.1 ml of their assigned treatment at the appropriate dose (0.2 ug for sPS and 1 CU for bPS). If no allergic reaction occurs within one minute, the participants will continue in the study and receive the full remaining dose over one minute. Participants will be evaluated one week before and four weeks after infusion for social, communication, and behavioral functioning as measured by Autistic Diagnostic Observation Schedule Generic (by blinded raters); Rimland Questionnaires (by parents and teachers); Expressive Vocabulary Test; MacArthur Communication Inventory (by parents and teachers); and Aberrant Behavior Checklist (by parents and teachers). Participants will also have a physical exam and blood and urine tests. After completion of preliminary data analysis, placebo patients will be offered open label therapy if appropriate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autism
Keywords
Pervasive Developmental Disorders, Secretin, synthetic porcine, Secretin, biological porcine, Autism Diagnostic Observation Schedule - Generic (ADOS-G), Rimland Questionnaire, Expressive Vocabulary Test, MacArthur Communication Inventory, Aberrant Behavior Checklist

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
Double
Allocation
Randomized
Enrollment
85 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
secretin, synthetic porcine
Intervention Type
Drug
Intervention Name(s)
secretin, biologically derived porcine

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Autism based on DSM-IV criteria IQ > 35 Medically fit for the study in the judgment of the study officials Exclusion Criteria Prior administration of secretin Acute or chronic pancreatitis Use of anticholinergics within 72 hours of study entry or anticipated need for anticholinergics during study Allergies to pork products Use of investigational drug within 1 month of study entry Change in any medication or other therapeutic modality being used to treat any neurodevelopmental or gastrointestinal symptoms of the underlying autism disorder within 1 month of study entry Any medical condition which, in the judgment of the investigator, would make the patient unable to safely participate in the study or comply with all study procedures Any medical diagnosis which could account for autistic spectrum disorder (i.e., Rett syndrome, Fragile X, tuberous sclerosis, disintegrative disorder, epilepsy, Landau Kleffner, other mental retardation syndromes, or history of severe motor delays or current sensory or motor impairment such as cerebral palsy) Hearing or visual impairments Use of psychotropic medications (except for occasional symptomatic use for sleep, etc.) within 6 months of study entry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alan Unis, MD
Organizational Affiliation
University of Washington
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Geraldine Dawson, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Edward Goldson, MD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sally Rogers, PhD
Organizational Affiliation
University of Colorado, Denver
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital
City
Denver
State/Province
Colorado
ZIP/Postal Code
80218
Country
United States
Facility Name
Center on Human Development and Disability
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195-1525
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
12410073
Citation
Unis AS, Munson JA, Rogers SJ, Goldson E, Osterling J, Gabriels R, Abbott RD, Dawson G. A randomized, double-blind, placebo-controlled trial of porcine versus synthetic secretin for reducing symptoms of autism. J Am Acad Child Adolesc Psychiatry. 2002 Nov;41(11):1315-21. doi: 10.1097/00004583-200211000-00012.
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Secretin for the Treatment of Autism

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