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NCT00628199 Clinical Trial

Study to Create Potential Cell-Based Therapies to Treat Human Disease and Disability

Infertility Clinical Trial

Official title:
Derivation of Primary Donor Cell Lines for Human Cell Reprogramming

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT00628199
Other study ID # SU-12202007-950
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date September 2007
Est. completion date January 2030

Study information
Verified date August 2022
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a research study in which your cells will be used for somatic cell nuclear transfer (SCNT), and/or genetic reprogramming research which may result in the production of stem cell lines. This study does not provide treatment.

Description:

It is thought that studies of genetic reprogramming and SCNT using human cells have the potential to give us new basic knowledge about human development. Current work will focus on developing this basic knowledge. In the future, human embryonic stem cell lines (hESC) derived from genetic reprogramming and SCNT may also have the potential to develop into cell types that are useful for cell-based therapies to treat human disease and disability.

Other known NCT identifiers
  • NCT00553826

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 60
Est. completion date January 2030
Est. primary completion date January 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 1 Year to 75 Years
Eligibility Inclusion Criteria:1. Donors with a degenerative disease phenotype or genetic disorders such as Type I Diabetes, heart disease, or infertility (azoospermia and premature ovarian failure) Exclusion Criteria:1. Unable to read or understand English. 2. Unable to provide skin biopsy sample due to skin condition in the underarm area.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Improving the scientific process of human cell reprogramming

Locations
Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

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