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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03251430
Other study ID # 17061943
Secondary ID
Status Recruiting
Phase N/A
First received August 7, 2017
Last updated January 8, 2018
Start date September 20, 2017
Est. completion date March 31, 2019

Study information

Verified date January 2018
Source Nagasaki University
Contact Shinichiro Kobayashi, MD
Phone 81958197316
Email shinichirokobayashi@nagasaki-u.ac.jp
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Osteoporosis after gastrectomy, which is characterized by both the loss of bone mass and the deterioration of bone architecture, is a serious complication in the long course after gastrectomy. The aim of the present study was to evaluate osteoporosis by using high-resolution peripheral quantitative computed tomography (HR-pQCT) in the long course after gastrectomy. In total gastrectomy and distal gastrectomy groups, at least 5 years should have elapsed since gastrectomy.


Description:

The patients after gastrectomy loss appetite and decrease the weight. Total gastrectomy especially cause severe sarcopenia and metabolic change. Osteoporosis after gastrectomy, which is characterized by both the loss of bone mass and the deterioration of bone architecture, is a serious complication in the long course after gastrectomy. The primary tools for assessing volumetric density and bone structure are quantitative computed tomography (QCT) and more recently, high-resolution peripheral quantitative computed tomography (HR-pQCT). However the validation of osteoporosis with HR-pQCT in the long course after gastrectomy remain elusive. The aim of the present study was to evaluate osteoporosis by using HR-pQCT in the long course after gastrectomy. In total gastrectomy and distal gastrectomy groups, at least 5 years should have elapsed since gastrectomy.


Recruitment information / eligibility

Status Recruiting
Enrollment 114
Est. completion date March 31, 2019
Est. primary completion date March 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 60 Years to 90 Years
Eligibility Inclusion Criteria:

- At least 5 years have elapsed since DG or TG due to gastric cancer

- Provide signed informed consent

Exclusion Criteria:

- pregnancy

- Current use of the following osteoporosis agents; Teriparatide, Denosumab, and bisphosphonate

- Hyperthyroidism

- Hyperparathyroidism

- Present malignancy (except in situ carcinoma)

- Any condition that required chronic (greater than three months cumulative and greater than 5 mg/day) glucocorticoid therapy

- Other diseases which affect bone metabolism

- Any disorder that, in the opinion of the investigator, may compromise the ability of the subject to give written informed consent and/or comply with study procedures

- Received > 3 months (or equivalent) of osteoporosis treatment

- Currently enrolled in or has not yet completed at least 1 month since ending other investigational device or drug trial(s), or subject is receiving other investigational agent(s).

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
gastrectomy
Distal gastrectomy, Total gastrectomy

Locations

Country Name City State
Japan Nagasaki University Hospital Nagasaki

Sponsors (1)

Lead Sponsor Collaborator
Kobayashi Shinichiro

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparing bone microstructure in control, DG, and TG groups volumetric bone mineral density day1
Secondary Comparing bone microstructure with sarcopenia Correlation between bone mineral density in HR-pQCT and cross-sectional area of the abdominal psoas major muscle day1
Secondary Comparing bone microstructure with serum biomarkers of osteoporosis Correlation between bone mineral density in HR-pQCT and biomarkers (25-hydroxyvitaminD, calcium, iPTH, P1NP, ICTP, TRACP5b) day1
Secondary Comparing bone microstructure with dual-energy X-ray absorptiometry Correlation of bone mineral density between HR-pQCT and DXA day1
Secondary Comparing bone microstructure with quality of life (QOL-C30) Patients will be asked to complete a short debriefing questionnaire covering questions (QOL-C30) day1
Secondary Comparing bone microstructure with quality of life (BDHQ) Patients will be asked to complete a short debriefing questionnaire covering questions ( BDHQ) day1
Secondary Comparing bone microstructure with quality of life (FRAX) Patients will be asked to complete a short debriefing questionnaire covering questions (FRAX) day1
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