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临床试验/CTRI/2025/04/084162
CTRI/2025/04/084162尚未招募不适用

A Study To Evaluate The Efficacy Of Ayurvedic Oil Massage As An Add On Therapy To Whole System Of Ayurveda In Cases Of Knee Osteoarthritis A Randomized Placebo Controlled Trial

State Ayurvedic College And Hospital ,Lucknow1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年1月5日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. Pain intensity in affected joint: determined visual analogue scale.

研究概览

简要总结

The Present Synopsis Entitled" “A study to evaluate the efficacy of ayurvedic oil massage as an add on therapy to whole system Ayurveda in cases of knee osteoarthritis: a randomized placebo controlled trial.”

AIM OF STUDY

To find out the additional benefits of massage therapy with medicated oil in comparison to placebo oil on the patients of Janugata Sandhivata /knee O.A. to receiving the whole system ayurveda intervention.

OBJECTIVES

 

Primary objective

To asses if additional benefits of medicated oil massage in comparison to placebo oil along with whole system of ayurveda in its functional outcome.

Secondary objective

1 To develop standard protocol for oil massage in knee osteoarthritis for its maximum efficacy.

2 Evaluating the cost implication.

3 Investigating potential adverse effects.

4 Assessing patient compliance.

PLAN OF STUDY

Selection of cases

  1. For the purpose of clinical trial, the patients of Janugata Sandhivata / knee O.A will be selected regardless of sex with will be selected randomly from O.P.D, I.P.D and Advanced Arthritis Research Clinic at state ayurvedic college and hospital, Lucknow and also the referred cases which fulfill the criteria.

  2. A careful history, physical examination and necessary investigation will be performed as Performa prepared for the present trial.

Type of study

Two arm parallel randomized controlled study.

SAMPLE SIZE

Minimum 60 patients with approximately 10% of dropouts of Janugata Sandhivata from OPD, IPD and advance arthritis research Centre at SAC & H will be selected & divided into two groups with the help of computer-generated random table.

Group A  In this group patients will be treated with whole system of ayurveda and massage with active medicated oil (Bala Ashwagandhadi oil)

Group B  In this group patients will be treated with whole system of ayurveda and massage with placebo controlled oil (Till tail)

INCLUSION CRITERIA

Patients who will be coming for the treatment of knee O.A in Kayachikitsa OPD and A-ATARC OPD.

Patients who will be diagnosed as having knee O.A on the basis of their clinical and radiological features.

Age  31 to 60 years.

Sex Both Male & Female.

Patients who have not taken any ayurvedic treatment earlier.

All Socio economic status

Patients who will give consent to participate in the study.

Radiological evidence of osteoarthritis of the knee joints up to grade3.

EXCLUSION CRITERIA

Patients below 31 years and above 60 years of age.

Patients having severe destructive radiological changes.

Patients suffering from rheumatoid arthritis, gouty arthritis, psoriatic arthritis, and infective arthritis.

Patients who have joint-related diseases other than knee osteoarthritis (OA)

Patients with history of trauma, septic arthritis and post traumatic knee pain etc.

Patients with osteoarthritis of knee joint of grade 4 and other systematic disorders.

Unwilling patients will be excluded.

GROUPING OF PATIENTS

Group A – In this group patients will be treated with whole system of ayurveda and massage with active medicated oil (Bala Ashwagandhadi oil)

Group B – In this group patients will be treated with whole system of ayurveda and massage with placebo controlled oil (Till tail)

  

Frequency and Duration

Frequency 5 days in a week.

Duration for 30 min.

Period of study

90 days (5 sitting in a week)

Follow up during trial period- At 30 days interval.

Follow up after the trial period- One month following the completion of the three-month trial.

CRITERIA OF ASSESSMENT

OBJECTIVE PARAMETER:

1 Pain intensity in affected joint: visual analogue scale.

2 Change in walking time for a fixed distance (pre &post comparison)

3 Hantisandhi ( range of movement of knee joints pre and post comparison)

SUBJECTIVE PARAMETER:

All the signs and symptoms are graded on the basis of their intensity and severity given by patients on complained and confirmed by clinical examination before intervention

The clinical improvement during and after the therapy will also be correlated with previous intensity of sign and symptoms.

A. COMMON CLINICAL SYMPTOMS

  1. Vatapurnadritisparsa (crepitus)

  2. Sandhi Shotha (joint swelling)

  3. Prasaran Akunchana pravriti savedana (pain during flexion and extension of joint)

  4. Tenderness of knee joints

  5. Morning stiffness (

RADIOLOGICAL ASSESSMENT OF KNEE (OA)

  1. Joint Space Narrowing

  2. Osteophytes Formation

  3. Subchondral Bone Sclerosis

Assessment of the result

Assessment of the result will be done on the basis of symptomatic relief and the changes in the objective, subjective and radiological parameters before and after the trial.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
31.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients who will be coming for the treatment of knee O.A in kaya chikitsa OPD and A-ATARC OPD.
  • Patients who will be diagnosed as having knee O.A on the basis of their clinical and radiological features.
  • Age: 31 to 60 years.
  • Sex: Both Male & Female.
  • Patients who have not taken any ayurvedic treatment earlier.
  • Socio economic status: All Patients who will give consent to participate in the study.
  • Radiological evidence of osteoarthritis of the knee joints up to grade3.

排除标准

  • Patients below 31 years and above 60 years of age.
  • Patients having severe destructive radiological changes.
  • Patients suffering from rheumatoid arthritis, gouty arthritis, psoriatic arthritis, and infective arthritis.
  • Patients who have joint-related diseases other than knee osteoarthritis (OA).
  • Patients with history of trauma, septic arthritis and post traumatic knee pain etc.
  • Patients with osteoarthritis of knee joint of grade 4 and other systemic disorders.
  • Unwilling patients will be excluded.

结局指标

主要结局

1. Pain intensity in affected joint: determined visual analogue scale.

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

2. Change in walking time for a fixed distance (pre &post comparison) Time

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

• Pre trial

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

• Post trial

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

3. Hantisandhi ( range of movement of knee joints pre and post comparison)

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

4. The Western Ontario and McMaster Universities Osteoarthritis Index

时间窗: Before trial, 30th day, 60th day, 90th day, after trial

次要结局

  • RADIOLOGICAL ASSESSMENT OF KNEE (OA) using the Kellgren-(Lawrence grading system)

研究者

发起方
State Ayurvedic College And Hospital ,Lucknow
申办方类型
Government medical college

研究点 (1)

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