Pilot RCT Using Homeopathic Medicines in ASD

NCT ID: NCT07161804

Last Updated: 2025-11-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE4

Total Enrollment

54 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2025-01-13

Brief Summary

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This study looked at whether homeopathic treatment could help children with Autism Spectrum Disorder (ASD) when used alongside regular therapies like speech and occupational therapy. Over seven years, children between the ages of 3 and 12 were divided into two groups (through computer generated list). One group received individualized homeopathic medicines, and the other received a look-alike placebo (with no active ingredients). Meanwhile, both the groups continued with their regular therapies.

Researchers used various tools and parent questionnaires to track the children's progress in areas like communication, behavior, social skills, daily functioning, toilet training and sensory skills.

Detailed Description

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Autism spectrum disorders (ASD) are lifetime neurodevelopmental disorders with challenges across functional domains. Despite availability of various treatment modalities and diagnostic tools, it's pathophysiology still remains poorly understood even through 8 decades of it's discovery. This pilot study compares psychometrics and parental reported outcome monitoring, behavioral and developmental outcomes, co-occurring breadth of concerns for children with ASD along with co-morbidities, with and without homeopathic treatment.

Methodology: Initial screening was done using Autism Behavior Checklist (ABC). Utilizing a randomized-controlled design and parental informed consent, this study compared children aged 3 to 12 years, divided into an experimental group receiving individualized homeopathic treatment alongside occupational/speech therapies (HG), and a control group receiving only latter (CG) .

The treatment group received homoeopathic medicines daily with frequency being once per day along with daily occupational / speech therapy sessions for 1 hour each. The control group received homoeopathic medicine look alike placebo daily with frequency being once per day along with daily occupational / speech therapy sessions for 1 hour each. Follow ups were done every 3 months and the data were combined and stored for each year separately for seven-years. The data was initially collected and then analyzed through standardized behavioral assessments \[Childhood Autism Rating Scale, CARS\] , speech-language assessments \[Social Responsiveness Scale, SRS\], parental-questionnaires for reporting emotional regulation, anxiety-related behaviors, co-morbidities \[Neuro Developmental Parent Report for Outcome Monitoring, ND-PROM\] and observational methods in both the groups. The treatment effectiveness was assessed using Autism Treatment Evaluation Checklist (ATEC).

Conditions

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Autism Spectrum Disorder (ASD)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Homoeopathic Group

Individualized Homoeopathic Medicines

Group Type EXPERIMENTAL

Homoeopathic medicines

Intervention Type DRUG

Thuja officinalis Vaccininum Causticum Argentum nitricum Tuberculinum Stramonium Staphysagria Arum triphyllum Bacillinum Cina Carcinocin Cuprum Metallicum Ambera grisea Calcarea carbonica Crocus sativus Hepar sulphur Hyoscymus Kali Bromatum Lac Vaccininum Medorrhinum Natrum phosphoricum Thyroidinum

Therapy

Intervention Type BEHAVIORAL

Occupational Therapy / Speech Therapy

Control Group

Placebo

Group Type PLACEBO_COMPARATOR

Therapy

Intervention Type BEHAVIORAL

Occupational Therapy / Speech Therapy

Placebo

Intervention Type DRUG

Saccharum lactis

Interventions

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Homoeopathic medicines

Thuja officinalis Vaccininum Causticum Argentum nitricum Tuberculinum Stramonium Staphysagria Arum triphyllum Bacillinum Cina Carcinocin Cuprum Metallicum Ambera grisea Calcarea carbonica Crocus sativus Hepar sulphur Hyoscymus Kali Bromatum Lac Vaccininum Medorrhinum Natrum phosphoricum Thyroidinum

Intervention Type DRUG

Therapy

Occupational Therapy / Speech Therapy

Intervention Type BEHAVIORAL

Placebo

Saccharum lactis

Intervention Type DRUG

Other Intervention Names

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Medicines

Eligibility Criteria

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Inclusion Criteria

* A confirmed diagnosis of Autism Spectrum Disorder (ABC score ≥ 67)
* Age range of 2 to 12 years

Exclusion Criteria

* Children with other significant comorbid psychiatric conditions that could confound the results. \[eg. a brain injury; fragile X syndrome or other syndromes resulting from known genetic defects or inherited metabolic diseases; other diagnosed conditions involving impairments in social and communication abilities, such as intellectual disability without ASD, global developmental delay, language disorders and social communication disorder\]
* Children with irregular follow ups.
* Children with poor medical compliance.
Minimum Eligible Age

2 Years

Maximum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Holistic Homoeopathic Clinic and Research Center

OTHER

Sponsor Role lead

Responsible Party

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Gyandas Wadhwani

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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GYANDAS G WADHWANI, MD (HOM.)

Role: PRINCIPAL_INVESTIGATOR

Holistic Homoeopathic Clinic and Research Center

Locations

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Holistic Homoeopathic Clinic and Research Center

New Delhi, SOUTH DELHI, India

Site Status

Countries

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India

Other Identifiers

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201724112024

Identifier Type: -

Identifier Source: org_study_id

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