Viewing Study NCT02411461


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Ignite Modification Date: 2026-02-23 @ 8:08 PM
Study NCT ID: NCT02411461
Status: COMPLETED
Last Update Posted: 2019-11-13
First Post: 2015-02-25
Is Gene Therapy: True
Has Adverse Events: True

Brief Title: Early-onset Obesity and Cognitive Impairment in Children With Pseudohypoparathyroidism
Sponsor: Vanderbilt University Medical Center
Organization:

Study Overview

Official Title: Early-onset Obesity and Cognitive Impairment in Children With Pseudohypoparathyroidism
Status: COMPLETED
Status Verified Date: 2019-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Pseudohypoparathyroidism type 1a (PHP1a) is a rare disease that causes childhood obesity and learning difficulties. This study will investigate eating behaviors and perform cognitive testing on children with PHP1a. The investigators will compare their results to those of healthy siblings and other obese children.
Detailed Description: Pseudohypoparathyroidism type 1a (PHP1a) is a genetic disorder that causes early-onset, syndromic obesity and cognitive impairment. This study aims to evaluate eating behaviors, cognition and executive function in children with PHP1a, compared with healthy siblings and matched obese controls.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
1K23DK101689-01A1 NIH None https://reporter.nih.gov/quic… View