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Clinical Trials/NCT01824797
NCT01824797
Completed
Not Applicable

Determining Changes in Bone Metabolism After Bariatric Surgery in Postmenopausal Women

Duke University1 site in 1 country42 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Duke University
Enrollment
42
Locations
1
Primary Endpoint
Changes in Bone Mineral Density
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose and objective of this study is to determine the changes in bone metabolism after bariatric surgery in postmenopausal women.

This is a prospective cohort study that will enroll up to 40 postmenopausal female subjects with class II and III obesity from the Duke Center for Metabolic and Weight Loss Surgery. The study team will enroll subjects that are already being scheduled for either sleeve gastrectomy or Roux-en-Y gastric bypass. The osteoclast activity, the osteoblast activity, and the bone mineral density will be measured in all subjects preoperatively and 12 months postoperatively through research specific blood tests and Dual energy x-ray Absorptiometry (DEXA) scans.

The primary endpoints are change in osteoclast activity as measured by C-terminal telopeptide of type I collagen and change in bone density as measured by DEXA scan. These are continuous variable and given the small sample size the investigators will use a nonparametric Wilcoxon rank-sum test to compare the difference in one year change in these variables. There is a slight risk of loss of confidentiality. Every effort will be made to protect all PHI. There is also the risk of increased exposure to radiation from the DEXA scans performed twice with each subjects participating in the study.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
May 31, 2018
Last Updated
6 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Postmenopausal women as determined by having a history of no menstrual bleed for greater than one year.
  • Body Mass Index ≥35 kg/m² and stable weight for the previous 3 months.
  • Able to speak and read English.
  • Being scheduled for either Roux-en-Y gastric bypass or sleeve gastrectomy.

Exclusion Criteria

  • A documented history of osteoporosis or currently receiving medical treatment for osteoporosis with bisphosphonates, teriparatide, raloxifene, or denosumab.
  • Weight greater than 295 pounds as this is the weight limit for our Dual-energy X-ray absorptiometry machine.
  • Current or past (less than 1 year from enrollment) usage of estrogen hormone replacement therapy.
  • Current smoker
  • Any history of glucocorticoid use greater than one year in duration or current use of glucocorticoids.

Outcomes

Primary Outcomes

Changes in Bone Mineral Density

Time Frame: Baseline to one year postoperative

Changes in bone mineral density will be determined by comparing a peroperative DEXA scan with a one year postoperative DEXA scan on postmenopausal subjects who have already planned to undergo Roux-en-Y gastric bypass or sleeve gastrectomy.

Secondary Outcomes

  • Biochemical Changes in Bone Metabolism(Baseline to one year postoperative)

Study Sites (1)

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