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临床试验/NCT07183215
NCT07183215Enrolling By Invitation2 期

Efficacy Test of Curcuminoid Standardized Turmeric Capsules to Improving Inflammatory Biomarkers in Osteoarthritis Genu

Gadjah Mada University1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2025年6月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
Enrolling By Invitation
发起方
入组人数
72
试验地点
1
主要终点
Secretion of TNF Alpha

研究概览

简要总结

The goal of this clinical trial is to learn if Curcuminoid Standardized Turmeric Capsules works to treat Osteoarthritis Genu in adults. It will also learn about the safety of Curcuminoid Standardized Turmeric Capsules. The main questions it aims to answer are:

  • Does Curcuminoid Standardized Turmeric Capsules lower the pain, TNF-Alpha, Interleukin-1 and CRP in the blood?
  • What medical problems do participants have when taking Curcuminoid Standardized Turmeric Capsules? Researchers will compare Curcuminoid Standardized Turmeric Capsules to a placebo to see if Curcuminoid Standardized Turmeric Capsules works to treat Osteoarthritis Genu.

Participants will:

  • Take Curcuminoid Standardized Turmeric Capsules or a placebo every day for 3 weeks
  • Visit the clinic once every week for checkups and tests
  • Keep a diary of their symptoms and the number of times they use a rescue paracetamol

详细描述

Evaluate the efficacy, safety, and tolerability of standardized curcuminoid from turmeric extract to TNF-Alpha, Interleukin-1 and CRP in elderly patients with Osteoarthritis Genu. This research is also to evaluate the effect of acupressure and standardized curcuminoid from turmeric extract vs placebo at three weeks : Knee pain as measured by the VAS score. Study design is randomized controlled trial, double-blind to assess efficacy, tolerability, and safety curcuminoid versus placebo. Patients can be pre-screened for specific x-ray and laboratory parameters. Eligible subjects will enter the washout for one week following a screening visit. After the washout period, eligible subjects will be randomized and treated for three weeks. The total duration of the study is up to 5 weeks. The primary efficacy variable is the number of TNF-Alpha, Interleukin-1 and CRP in blood, collected at Week 4 to BL (i.e., change from BL in the number of Leukocytes at Week 4). It will be analyzed using the Wilcoxon signed-rank test or paired t-test and the Mann-Whitney U test or independent t-test. The significance level will be set at 0.05. All outcome measures will be recorded at baseline and after two weeks of intervention

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
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • Clinical diagnosis of Osteoarthritis which confirmed by physical examination and x-rays
  • Experience pain with a Numeric Rating scale of 1-7
  • Must be able to swallow capsules
  • Must be able to carry out mobility without assistance or with minimal assistance

排除标准

  • Parkinson's disease
  • Dementia disease
  • Psychosis disease
  • Joint dislocations
  • Rheumatic diseases other than Osteoarthritis (rheumatoid arthritis)
  • Undergoing joint replacement therapy.
  • Analgesic dependent disease

研究组 & 干预措施

Intervention Group

Experimental

Capsules containing curcuminoid from Tumeric Extract three times a day for 3 weeks

干预措施: Curcuminoid Standardized Turmeric Capsules (Drug)

Control Group

Placebo Comparator

Capsules containing maltose three times a day for 3 weeks

干预措施: Placebo (Other)

结局指标

主要结局

Secretion of TNF Alpha

时间窗: 3 weeks

TNF alpha is a cytokine, a protein that plays a role in the immune system and inflammation. TNF alpha is produced by various types of cells, particularly activated macrophages, and plays a role in various biological processes such as inflammation and immunity against infection. The cytokine TNF alpha is an essential mediator in increasing the inflammatory response, which can be detected in the blood plasma of patients with Osteoarthritis. The TNF alpha examination was conducted using the Enzyme Linked Immunosorbent Assay (ELISA) method on blood plasma

Secretion of the Interleukin-1

时间窗: 3 weeks

Interleukin-1 is a pro-inflammatory cytokine that plays a key role in immune and inflammatory responses, produced primarily by macrophages. IL-1 can cause fever, increase blood vessel permeability, and trigger bone and cartilage damage. The cytokine Interleukin-1 is an essential mediator in increasing the inflammatory response, which can be detected in the blood plasma of patients with Osteoarthritis. The Interleukin-1 examination was conducted using the Enzyme Linked Immunosorbent Assay (ELISA) method on blood plasma

Secretion of C Reactive Protein

时间窗: 3 weeks

C-reactive protein (CRP) is a blood marker for inflammation in the body, produced by the liver in response to infection, injury, or autoimmune conditions. A simple blood test measures CRP levels, with higher concentrations indicating greater inflammation. C-reactive protein (CRP) is measured with a blood test to detect and monitor inflammation in your body. A blood sample is taken from a vein and analyzed in a laboratory to determine the CRP level. The results are reported in milligrams per liter (mg/L), and higher than normal levels indicate inflammation that may be caused by infection, injury, or a chronic condition.

次要结局

  • Change of Pain(3 weeks)

研究者

发起方
Gadjah Mada University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Srinalesti Mahanani

Dr.

National Institute of Health Research and Development, Ministry of Health Republic of Indonesia

研究点 (1)

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