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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT03203941
Other study ID # HSC-MS-17-0529
Secondary ID
Status No longer available
Phase
First received
Last updated

Study information

Verified date May 2020
Source The University of Texas Health Science Center, Houston
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

Individual patient expanded access protocol for a child with cerebral palsy (CP) who has autologous umbilical cord blood available and who is ineligible to participate in other stem cell studies for children with CP.


Description:

This protocol is part of an FDA Individual Patient Expanded Access IND submitted at the request of the parents of a child with cerebral palsy (CP) who is ineligible to participate in other stem cell studies. For this child, there are no other treatment options.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

-

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Autologous Cord Blood Stem Cells
This is an individual patient expanded access protocol.

Locations

Country Name City State
United States The University of Texas Health Science Center at Houston Houston Texas

Sponsors (1)

Lead Sponsor Collaborator
Charles Cox

Country where clinical trial is conducted

United States, 

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