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临床试验/NCT04321837
NCT04321837已完成2 期

Coral Calcium's Effect on Bone Density in Postmenopausal Women With and Without Ibandronate

Columbia University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年2月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Mean change in bone mineral density (BMD) (lumbar spine)

研究概览

简要总结

This study will investigate the effect of coral calcium complex supplementation on BMD of osteoporotic individuals either when used alone or in combination with ibandronate. Ibandronate alone will also be tested in comparison to coral calcium supplementation alone or in combination.

详细描述

Osteoporosis and resulting fragility fractures are major causes of morbidity and mortality in older individuals. Current estimates indicate that as many as 50% of American women and 20% of men over the age of 50 will be at risk for osteoporotic fractures during their lifetimes, and that these fractures are associated both with higher risk for further fractures and with higher mortality rates. Osteoporosis and subsequent fragility fractures can be prevented if diagnosed and treated appropriately. The first step of treatment guidelines for individuals with reduced bone mineral density (BMD), as identified with dual energy x-ray absorptiometry (DXA) scan, is the implementation of lifestyle measures to reduce bone loss. These include the supplementation of dietary calcium and vitamin D to maintain appropriate calcium intake and reduce resorption of mineralized calcium from bone. Pharmacological treatment can be used for the treatment of osteoporosis in individuals who have reduced BMD (less than -2.5 T-score) and for those who have sustained a fragility fracture. The bisphosphonates are first line agents for the treatment of osteoporosis. Coral-derived calcium is a novel formulation of calcium supplement, which has not yet been rigorously investigated as an efficacious nutrient for the skeleton. Ibandronate is a commonly available bisphosphonate prescribed for the treatment of osteoporosis. Vitamin D is a nutrient required to absorb vitamin D from the diet.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Postmenopausal women, 50-75 years of age (inclusive). Menopause is defined as no menstrual period for 1 year.
  • BMD T-score of lumbar spine (L1-L4), femoral neck, total hip, or non-dominant forearm < -2.5 as determined by DXA.

排除标准

  • T-score of lumbar spine, femoral neck, total hip, or non-dominant forearm < -3.
  • Use of any supplemental calcium preparations in the past 1 year.
  • Use of ibandronate in the past 3 years.
  • Current use of
  • prednisone or other corticosteroid,
  • antiseizure medications,
  • thiazide diuretics, or
  • estrogen preparation except vaginal cream.
  • Electrolyte abnormalities, as defined by abnormal blood levels of sodium (Na), chlorine (Cl), potassium (K), phosphate (Phos), calcium (Ca), or magnesium (Mg) values on initial screen.
  • Chronic disease, including
  • liver disease (as defined by elevated blood levels of aspartate aminotransferase, alanine aminotransferase, and/or alkaline phosphatase or reduced albumin or total protein on initial screen),
  • stage III renal disease or worse (as defined by epidermal growth factor receptor (eGFR) < 60 cc/min),
  • abnormal thyroid function tests,
  • current parathyroid disease (as defined by hypercalcemia and elevated levels of parathyroid hormone (PTH) - if history of hyperparathyroidism, surgical cure has to be documented more than 5 years ago),
  • diabetes mellitus,
  • any other known metabolic bone disease besides osteoporosis, and/or
  • any inflammatory, anatomic, or malabsorptive GI tract disease.
  • Osteoporotic fracture in the past 6 months, defined as a low-energy fracture such as a fracture after falling from a standing height.

研究组 & 干预措施

Coral calcium complex and ibandronate

Active Comparator

干预措施: Coral Complex 3 (Dietary Supplement)

Coral calcium complex and ibandronate

Active Comparator

干预措施: Ibandronate (Drug)

Ibandronate and vitamin D

Active Comparator

干预措施: Ibandronate (Drug)

Ibandronate and vitamin D

Active Comparator

干预措施: Vitamin D3 (Dietary Supplement)

Coral calcium complex

Active Comparator

干预措施: Coral Complex 3 (Dietary Supplement)

结局指标

主要结局

Mean change in bone mineral density (BMD) (lumbar spine)

时间窗: 48 weeks

Participant bone mineral density of lumbar spine.

Mean change in BMD (femoral neck)

时间窗: 48 weeks

Participant bone mineral density of femoral neck.

Mean change in BMD (forearm)

时间窗: 48 weeks

Participant bone mineral density of forearm.

Mean change in BMD (total hip)

时间窗: 48 weeks

Participant bone mineral density of total hip.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John P. Bilezikian

Dorothy L. and Daniel H. Silberberg Professor of Medicine and Professor of Pharmacology

Columbia University

研究点 (1)

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