NCT00328731

Brief Summary

We sought to determine the efficacy of NAET® in permanently eliminating milk allergy for a sample of patients. We hypothesize that the subjects in the experimental group will show similar level of allergies and sensitivities initially on all nine diagnostic measures used here. After receiving the NAET treatments, the Experimental group will demonstrate a significant reduction in the milk sensitivities and allergies when compared to the control group at the final evaluation using same diagnostic measures.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
26

participants targeted

Target at P25-P50 for phase_1

Timeline
Completed

Started Jan 2005

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2005

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2006

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

May 19, 2006

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 22, 2006

Completed
Last Updated

May 22, 2006

Status Verified

January 1, 2005

First QC Date

May 19, 2006

Last Update Submit

May 19, 2006

Conditions

Milk Allergy

Keywords

AllergyNAET

Outcome Measures

Primary Outcomes (1)

  • Reduction of Milk allergies

Secondary Outcomes (1)

  • This study also evaluated the reliability of performing two testing procedures (NST & PDRS) by two independent examiners in testing the subjects for milk at two different times.

Interventions

ProcedurePROCEDURE

Eligibility Criteria

Age18 Years - 78 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Known milk allergy, sensitivity or intolerances. -

You may not qualify if:

  • No milk allergy or sensitivity H/o Anaphylaxis or severe reactions Any other major illnesses preventing from taking part in any study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

NAET-Pain Clinic

Buena Park, California, 90621, United States

Location

MeSH Terms

Conditions

Milk HypersensitivityHypersensitivity

Interventions

Methods

Condition Hierarchy (Ancestors)

Food HypersensitivityHypersensitivity, ImmediateImmune System Diseases

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Officials

  • Devi S Nambudripad, DC,PhD,L.Ac

    NAR Foundation

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
DOUBLE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

May 19, 2006

First Posted

May 22, 2006

Study Start

January 1, 2005

Study Completion

January 1, 2006

Last Updated

May 22, 2006

Record last verified: 2005-01

Locations

US(1)