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临床试验/NCT05381168
NCT05381168Unknown不适用

Efficacy and Safety of Calcium From Fish Bone in Volunteers With Osteopenia

Chulalongkorn University0 个研究点目标入组 48 人开始时间: 2022年5月20日最近更新:
适应症

试验速览

阶段
不适用
入组人数
48
主要终点
Bone mineral density score

研究概览

简要总结

The aims of this study are to explore efficacy and safety of calcium from fish bone in volunteers with osteopenia. The volunteers are divided into 2 groups which are calcium from fish bone treatment group and calcium carbonate treatment group. Both groups received the calciums everyday for 6 months. Bone mineral density, blood examination, physical examination, adverse events, and satisfaction are evaluated before and after treatment.

详细描述

The aims of this study are to explore efficacy and safety of calcium from fish bone in volunteers with osteopenia. The volunteers are divided into 2 groups which are calcium from fish bone treatment group and calcium carbonate treatment group. Both groups received the calciums everyday for 6 months. Bone mineral density is analyzed before and after treatment. Osteocalcin, total procollagen type-1 N-terminal propeptide (P1NP), beta-crosslaps, parathyroid hormone (PTH), calcium, phosphate level, vitamin D level (Serum 25(OH)D), albumin, aspartate transaminase (AST), alanine transaminase (ALT), alkaline phosphatase (ALP), creatinine (Cr), blood urea nitrogen (BUN), and complete blood count (CBC) are assessed before and after taking for 3 and 6 months. Physical performance and food diary are also tested and records. Moreover, adverse effects including skin allergy, gastrointestinal abnormality, respiratory abnormality are evaluated. Satisfaction is asked after treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Male age more than 70 years or female age more than 65 years or all age volunteers that have at least 1 risk factors which are menopause before 45 years, menopause with the height reduction (more than 4 cm), body mass index less than 20 kg/mm2, bone fracture history, taking some medicine that has an effect on bone density reduction, have disease that has an effect on bone density reduction, Father and mother have bone fracture history, fracture risk assessment tool (FRAX) in intermediate risk, osteoporosis self-assessment tool for asian (OSTA) score, khon kaen osteoporosis study (KKOS) score in intermediate risk or higher intermediate risk
  • Bone mineral density between -1 to -2.5
  • No osteosclerosis
  • Can read and write
  • Willing to be volunteer

排除标准

  • Allergic to calcium, magnesium, phosphorus, zinc, collagen, and osteocalcin
  • Taking calcium or vitamin D with in 14 days before the study start
  • Taking osteosclerosis' medicine
  • Have uncontrolled diseases
  • Pregnancy and lactation
  • Participating in other study

结局指标

主要结局

Bone mineral density score

时间窗: 6 months

Bone mineral density score is measured using dual energy x-ray absorptiometry scanner (DEXA scanner). It shows in term of T-score. The outcomes are compared bone mineral density score of calcium from fish bone group to calcium carbonate group.

次要结局

  • Blood urea nitrogen level(6 months)
  • Vitamin D level(6 months)
  • Blood calcium level(6 months)
  • Parathyroid hormone (PTH) level(6 months)
  • Short physical performance battery score(6 months)
  • Grip strength(6 months)
  • Satisfaction level(6 months)
  • Osteocalcin level(6 months)
  • Blood phosphate level(6 months)
  • Pain score(6 months)
  • Gastrointestinal tract abnormality(6 months)
  • Total procollagen type-1 N-terminal propeptide (P1NP) level(6 months)
  • Beta-crosslaps level(6 months)
  • Liver function level(6 months)
  • Creatinine level(6 months)
  • Skin allergic reactions(6 months)
  • Respiratory tract abnormality(6 months)

研究者

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

Pornanong Aramwit, Pharm.D., Ph.D

Professor

Chulalongkorn University

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