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临床试验/NCT04767841
NCT04767841撤回1 期

The AMPK Modulator Metformin as a Novel Adjunct to Conventional Therapy in Patients With Knee Osteoarthritis: A Proof-of-Concept, Randomized, Double-Blind, Placebo-Controlled Trial

Sadat City University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2021年2月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
发起方
入组人数
120
试验地点
1
主要终点
Visual Analogue scale assessment of pain

研究概览

简要总结

metformin alleviates drug-induced osteoarthritis (OA)-like change in mice knee joint through activating autophagy and downregulating apoptosis. Metformin exerts its protective effects against OA through the AMPKa2/ SIRT1 pathway. Metformin suppresses IL-1β-induced oxidative and osteoarthritis-like inflammatory changes by enhancing the SIRT3/PINK1/Parkin signaling pathway, thereby indicating metformin's potential in prevention and treatment of osteoarthritic joint disease.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Primary osteoarthritis Patients recruited were between 30 to 60 years of age, with X-ray confirmed Kellgren-Lawrence grade13 II or III severity primary tibiofemoral OA, according to the American College of Rheumatology criteria.

排除标准

  • Those patients were excluded from the present study who:
  • were of age less than 30 years or more than 60 years
  • presented with active concomitant gastroduodenal disorders, hepatic and renal impairment within last 30 days prior to receiving the study drug
  • were diagnosed to have any inflammatory arthritis, gout or acute trauma of the knee, hip or spine; accompanying OA of the hip of sufficient severity to interfere with the functional assessment of the knee
  • had previous or ongoing treatment with oral SYSDOA (e.g., glucosamine sulphate, chondroitin sulphate, diacerein, piascledine), anti-depressants, tranquillisers, antacids or antibiotics; were having active cardiac lesion or hypertension, were pregnant females and those who were planning their pregnancy during the study
  • were having a known hypersensitivity to the used medications
  • have persistent diarrhoea or laxative use; severe gastrointestinal disorders, severe obesity, severe parenchymal organ disease, or anaemia (haemoglobin< 10.0 g/ dl or haematocrit < 30%).
  • Patients who received oral, intramuscular, intraarticular or soft tissue injections of corticosteroids within last eight weeks before receiving the first dose of the study medication, or had undergone joint lavage and arthroscopic procedures in the previous 6 months, were also excluded.

研究组 & 干预措施

Metformin

Experimental

Metformin 1000 mg daily plus Celecoxib 200mg capsule

干预措施: Metformin (Drug)

Placebo

Experimental

Placebo tablet daily plus Celecoxib 200mg capsule

干预措施: Placebo (Drug)

结局指标

主要结局

Visual Analogue scale assessment of pain

时间窗: week 12

the change of Visual Analogue Scale (VAS) pain score from baseline to posttreatment

次要结局

  • AMPK expression(12 weeks)
  • WOMAC change(week 12)
  • Serum level Tumor necrosis factor- alpha (TNF-α)(12 weeks)
  • the change of Short Form 36 Questionnaire (SF-36) score from baseline to posttreatment(week 12)
  • IL-17(12 weeks)
  • Adverse drug reaction(12 weeks)
  • Serum levels of IL-1β(12 weeks)

研究者

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

Mahmoud Samy Abdallah

Principle Investigator

Sadat City University

研究点 (1)

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