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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01398774
Other study ID # 11-007972
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date June 2011
Est. completion date November 20, 2017

Study information

Verified date August 2018
Source Children's Hospital of Philadelphia
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators would like to learn more about the metabolic consequences of pseudohypoparathyroidism type 1a in children, adolescents and adults with this condition. People with pseudohypoparathyroidism 1a are at risk for development of obesity. To better understand the cause of overweight or obesity, investigators are measuring body composition and resting energy expenditure (REE), which is the amount of calories burned while completely at rest. The investigators also want to determine the amount of body fat.


Description:

Pseudohypoparathyroidism 1a (PHP1a) is a disorder that is associated with many endocrine problems. People with PHP1a are at risk for the development of obesity. The objective of the study will help determine if obesity is related to abnormalities energy expenditure, meaning that people with PHP1a may not burn as many calories while at rest as those without the disorder.

In order to further evaluate obesity in PHP1a, investigators are planning to measure resting energy expenditure (REE), which is the amount of calories burned while completely at rest. Investigators will also evaluate body composition by looking at measures of growth and development and determining the amount of body fat using dual energy x-ray absorptiometry (DXA) as well as blood and urine biologic markers of obesity. The investigators plan to evaluate people with PHP1a at all weights.


Recruitment information / eligibility

Status Terminated
Enrollment 519
Est. completion date November 20, 2017
Est. primary completion date September 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Years to 45 Years
Eligibility Inclusion Criteria:

- Diagnosis of pseudohypoparathyroidism 1a

- Any body weight

Exclusion Criteria:

- Absence of above diagnosis

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Children's Hospital of Philadelphia Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital of Philadelphia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Resting Energy Expenditure The subject will rest for 30 minutes in the lab prior to the start of the test. A 60-minute resting energy expenditure (REE) test will be performed between 7:00 and 10:00 A.M. with the subject resting quietly under a clear, plastic hood watching a videotape. 30 minutes
Secondary Characterize body composition in patients with PHP1a. Body composition outcomes will be characterized by whole body lean mass and fat mass sex- and race-specific z-scores relative to height. 12 months
See also
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Enrolling by invitation NCT04240821 - Theophylline for Treatment of Pseudohypoparathyroidism Phase 2
Completed NCT02463409 - Theophylline as a Treatment for Children With Pseudohypoparathyroidism Type 1a (Albright Hereditary Osteodystrophy) Phase 2
Terminated NCT03761290 - Glucose Homeostasis in Pseudohypoparathyroidism
Recruiting NCT04551170 - Theophylline Treatment for Pseudohypoparathyroidism - Children 2-12 Years Old Phase 2
Recruiting NCT00209235 - Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments N/A
Completed NCT02411461 - Early-onset Obesity and Cognitive Impairment in Children With Pseudohypoparathyroidism