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临床试验/NCT06828783
NCT06828783已完成不适用

Development of Anti-Ageing Health Supplement From Subcritical Water Extraction of Zingiber Officinale Roscoe (Ginger) Bioactive Compounds

National University of Malaysia2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年11月7日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
90
试验地点
2
主要终点
Muscle mass

研究概览

简要总结

This study examines the development and efficacy of a health supplement derived from ginger using water extraction. Designed to address aging-related issues such as muscle loss (sarcopenia) and cognitive decline, the capsule's safety and effectiveness were evaluated through clinical trials. Stability testing ensured the capsules maintained their quality under various environmental conditions. Clinical trials further assessed the supplement's antioxidant and anti-inflammatory properties. The findings support its potential benefits for elderly health and aging-related challenges.

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
Double (Participant, Investigator)

入排标准

年龄范围
48 Years 至 63 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy adult male
  • Blood chemistry results specifically Blood Urea Nitrogen (BUN), Serum Creatinine, Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT), Gamma-glutamyl transpeptidase (GGTP), Total Bilirubin and alkaline phosphatase and urinalysis results, specifically urine pH, protein, glucose, ketone, and bilirubin levels within +/- 20% of normal value indicated in the lab report.
  • Individuals are willing to maintain their exercise habits and dietary patterns throughout the trial
  • No allergy to ginger
  • Provide written informed consent before screening
  • Subject is willing and able to comply with the study visit schedule and procedure, geographic proximity (investigator's discretion) that allows adequate follow-up
  • Subjects understand the study protocol and sign informed consent forms

排除标准

  • Use of dietary supplements within one week of Day
  • Supplements include any ginger (Zingiber officinale, ginger root, black ginger, zingiberis rhizoma) vitamins, minerals, and herbal products, including herbal drinks.
  • Presence of, or clinically significant history of, cancer, cardiovascular, endocrine, kidney, liver, lung, gastrointestinal, metabolic disorder, absorption disorder such as Celiac or Crohn's disease and/or any other chronic health condition such as diabetes identified from the findings of the interview.
  • Presence of gallstones or history of gallbladder disease.
  • Presence or history of diabetes.
  • Presence of cardiovascular disease and hypertension with inconsistent medication regimen, unstable conditions, and without proper physician's - Ten hours before the blood and urine sample collection, subjects should refrain from using medications such as statins (e.g., simvastatin, fluvastatin), NSAIDS including paracetamol, aspirin, nitric oxide (eNOS) activators or inhibitors (e.g., selegiline, Viagra), and angiotensin II receptor blocker (e.g., Telmisartan (blood pressure)) or take any of these medications
  • Subjects with vegan diet
  • Current smoker or used to smoke in the past 3 months
  • Subject for surgery or had undergone surgery in the past 3 months History of bleeding tendencies or any condition predisposing to bleeding e.g. thrombocytopenia, abnormal liver function, liver disease (e.g. chronic hepatitis), gastrointestinal ulcers
  • Subjects who have significantly changed their physical activity in the past 2-4 weeks or who intend to change them during the study
  • Participation in another clinical trial within 30 days of enrolment into the study.
  • History or current abuse of nicotine, drugs, or alcohol, or intake > 3 alcoholic beverages per day

结局指标

主要结局

Muscle mass

时间窗: Baseline and 24 weeks after supplementation

Appendicular lean mass in kilograms, kg will be measured using Dual-Energy X-ray Absorptiometry, (DEXA)

Fat mass

时间窗: Baseline and 24 weeks after supplementation

Fat mass in gram, g will be measured using Dual-Energy X-ray Absorptiometry, (DEXA)

Bone mineral content (BMC)

时间窗: Baseline and 24 weeks after supplementation

Bone mineral content in gram, g will be measured using Dual-Energy X-ray Absorptiometry, (DEXA)

Gait speed test

时间窗: Baseline and 24 weeks after supplementation

Gait speed will be measured in meters per second (m/s). Participants will complete three walking trials, with each trial timed over a 6-meter distance to record gait speed in seconds.

Handgrip strength

时间窗: Baseline and 24 weeks after supplementation

Evaluation of hand grip strength will be conducted using a dynamometer. Participants will be instructed to grip the dynamometer. The values will be recorded in kilograms (kg)

Cognitive function

时间窗: Baseline and 24 weeks after supplementation

The assessment instrument, the Montreal Cognitive Assessment (MoCA) test will be administered. The evaluation involves assessing participants through questions and instructions covering executive and spatial cognitive domains. The maximum score is 30. A score of 26 and above indicates no cognitive impairment.

Recall memory function

时间窗: Baseline and 24 weeks after supplementation

The Rey Auditory Verbal Learning Test (RAVLT) will be utilized. The RAVLT includes two distinct word lists (A and B). Participants will recall the items from list A over five trials (Memory A1 to A5). Following this, an interference list (list B), comprising 15 unrelated nouns, will be introduced, and participants will attempt to recall as many words as possible from it. Subsequently, participants will be asked to recall the words from list A (Delayed recall/Memory A6) without the examiner repeating the list. The number of correctly recalled words for each trial will be totaled to generate a score. Total Learning Score (Sum of Trials A1-A5) to indicate normal performance: 45-65, Mild Cognitive Impairment: 30-45, dementia: below 30. For delayed recall score (M6), to indicate normal performance: ≥8-12 words recalled, Mild Cognitive Impairment: 4-7 words recalled, and dementia: ≤3 words recalled.

Working memory function

时间窗: Baseline and 24 weeks after supplementation

The Digit Span Test involves recalling numbers in the same order (forward), reverse order (backward), or ascending order (sequencing). The test starts with short sequences and increases in length to assess memory capacity. A higher score (20 - 30) indicates better cognitive function, while a lower score (0 - 19) may suggest attention or memory issues. The total score is 30.

次要结局

  • Blood pressure(Baseline and 24 weeks after supplementation)
  • C-Reactive protein (CRP)(Baseline and 24 weeks after supplementation)
  • Untargeted metabolomics for metabolite identification(Baseline and 24 weeks after supplementation)

研究者

发起方
National University of Malaysia
申办方类型
Other
责任方
Sponsor

研究点 (2)

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