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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01724489
Other study ID # 2012P002276
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2013
Est. completion date April 1, 2019

Study information

Verified date December 2019
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Obesity is an important risk factor for osteoporosis and fractures. With the growing prevalence of obesity in the U.S., understanding the pathophysiology of bone loss in this population is of importance to public health. Growth hormone (GH) is a critical mediator of bone homeostasis and is markedly reduced in obesity. Our preliminary data suggest an important role for the GH/insulin-like growth factor 1 (IGF-1) system in the pathogenesis of bone loss in obesity. The development of novel imaging techniques provides an opportunity to investigate the effects of GH on skeletal structure and strength, which will provide insights into the pathogenesis of obesity related bone loss. Understanding the pathophysiology of bone loss in obesity may help identify new treatment targets for this important complication. The investigator hypothesizes that low-dose GH administration for 18 months will improve skeletal health.


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date April 1, 2019
Est. primary completion date November 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Ages 18-65 and generally healthy

- BMI = 25 kg/m2

- Bone mineral density (BMD) T score = -1.0 and > -2.5 (as measured by DXA)

Exclusion Criteria:

- For women: amenorrhea for 3 months, pregnancy or breastfeeding, polycystic ovary syndrome

- History of diabetes mellitus, cancer or other serious chronic disease

- Use of osteoporosis medications

- Anemia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Growth hormone

Placebo


Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Massachusetts General Hospital National Institutes of Health (NIH), Pfizer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bone Mineral Density Change in BMD over 18 months in the GH vs placebo group baseline and 18 months
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