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临床试验/NCT05296993
NCT05296993Unknown2 期

The Safety and Effectiveness of the Extended Longevity Protocol on the Epigenetic Aging Rate in Healthy Individuals

TruDiagnostic2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2021年5月25日最近更新:
适应症

试验速览

阶段
2 期
发起方
入组人数
15
试验地点
2
主要终点
Epigenetic Age

研究概览

简要总结

The purpose of this study is to quantifiably determine if the Extended Longevity Protocol has a significant clinical effect on epigenetic age.

详细描述

This is a prospective non-randomized clinical study of 15 patients to determine if the safety and effectiveness of the Extended Longevity Protocol's impact on the nine determinant factors of aging can decelerate aging.

There is evidence that the Extended Longevity Protocol decelerates aging and the risk of age-related diseases. The aim of this pilot study is to evaluate the safety, efficacy and feasibility of the Extended Longevity Protocol as an effective treatment option to improve clinical care of healthy individual's biological age thus prolonging longevity.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • 8 Men and 7 Women
  • Must between 55-75 years old
  • Patient must be able to comply with treatment plan and laboratory tests
  • Patients must have adequate immune system function, with no known immunodeficiency disease

排除标准

  • Neoplastic cancer within 5 years prior to screening, except for cutaneous basal cell or squamous cell cancer resolved by excision
  • No immune system issues or immunodeficiency disease
  • No history of viral illness which could be reactivated by immune downregulation
  • Presence of clinically significant acute or unstable cardiovascular and cerebrovascular (stroke) disease
  • Diagnosis of a transient ischemic attack in the 6 months prior to screening
  • Patients infected with hepatitis, C or HIV
  • Patients with Body Mass Index (BMI) > 40 kg/m2
  • Presence of active infection
  • Any other illness, psychiatric disorder, alcohol or chemical dependence that in the opinion of the investigator would render a patient unsuitable to participate in the study
  • Unable or unwilling to provide required blood sample for testing

结局指标

主要结局

Epigenetic Age

时间窗: Testing will compare the change in results after completion of intervention with baseline

serum epigenetic aging test

次要结局

未报告次要终点

研究者

发起方
TruDiagnostic
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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