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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01836562
Other study ID # 00105
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received February 26, 2013
Last updated September 16, 2014
Start date September 2014
Est. completion date June 2016

Study information

Verified date September 2014
Source Chaitanya Hospital, Pune
Contact Sachin P Jamadar, D.Ortho
Phone +918888788880
Email sac2751982@gmail.com
Is FDA regulated No
Health authority India: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This clinical trial is a single Arm, single centre to check the safety and efficacy of bone marrow derived autologous mono nuclear cells (MNC) (100 million per dose). Trial to be conducted for 36 months.


Description:

Autism is a developmental disorder that appears in the first 3 years of life, and affects the brain's normal development of social and communication skills. Autism is a physical condition linked to abnormal biology and chemistry in the brain. The exact causes of these abnormalities remain unknown,Symptoms-Children with autism typically have difficulties in: Pretend play, Social interactions, Verbal and non-verbal communication. Some children with autism appear normal before age 1 or 2 and then suddenly "regress" and lose language or social skills they had previously gained. This is called the regressive type of autism. People with autism may: Be overly sensitive in sight, hearing, touch, smell, or taste.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 3 Years to 70 Years
Eligibility Inclusion Criteria:

- Patient should suffer from Autism.

- willingness to undergo bone marrow derived autologous cell therapy.

- patient those provide fully Informed consent form for the study.

- Ability and willingness to regular visit to hospital and follow up during the protocol Procedures.

Exclusion Criteria:

- Patients with pre - existing or Current systemic disease such as lung , liver ( exception; History of uncomplicated Hepatitis A),gastrointestinal, Cardiac , Immunodeficiency,(including HIV) Or laboratory Investigation that could cause a neurological defect.History of Life threatening Allergic or immune- mediated reaction.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Biological:
STEM CELL THERAPY
Intra thecal injection of autologous MNC ,Intra thecal inj.of 100 millions MNC in 3 doses at 10 days interval.

Locations

Country Name City State
India Chaitanya Hospital Pune Maharashtra

Sponsors (1)

Lead Sponsor Collaborator
Chaitanya Hospital, Pune

Country where clinical trial is conducted

India, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in childhood autism rating scale 6 month Yes
Secondary Improvement in perfusion of brain with PET scan report 6 MONTH Yes
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