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临床试验/CTRI/2025/12/098267
CTRI/2025/12/098267尚未招募2 期

Comparative Clinical Validation study of Unani Pharmacopoeial formulation Itrifal-e-Muqil Mullaiyan & Roghan e Babuna Qawi vs Habb-e-Suranjan & Roghan e Suranjan in Waja ul Mafasil (Rheumatoid Arthritis)

Central Council for Research in Unani Medicine CCRUM New Delhi3 个研究点 分布在 1 个国家目标入组 210 人开始时间: 2025年12月10日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
210
试验地点
3
主要终点
The safety and efficacy of Unani Pharmacopeial formulation Itrifal-e-Muqil Mullaiyan & Roghan e Babuna Qawi in comparison with Habb-e-Suranjan & Roghan e Suranjan in Waja ul Mafasil (Rheumatoid Arthritis) will be carried out on the basis of DAS28 Form

研究概览

简要总结

Rheumatoid arthritis (RA) is a long-lasting inflammatory condition of undetermined causative factors with the hallmark of symmetric joint involvement. It is an autoimmune disorder in which the body’s immune system attacks its own tissue, including joints. Due to the synovial membrane being the primary target of RA, the synovium becomes inflamed and proliferates, articular cartilage is lost, and the bone is eroded. Waja ál-mafasil, an Arabic term made up of the terms "waja" for pain and "mafasil" for joint, is used to explain rheumatoid arthritis in Unani medicine. Waja ál-Mafasil is also referred to as "Hudar". The aim of this trial is assess the safety and efficacy of Unani pharmacopoeial formulation Itrifal-e-Muqil Mullaiyan & Roghan e Babuna Qawi vs Habb-e-Suranjan & Roghan e Suranjan in patients of Waja-ul mafasil (Rheumatoid Arthritis). This study is designed as a Multi centric, Randomized, Parallel Group, Active Controlled trial in patients with Waja ul Mafasil (Rheumatoid Arthritis) . After screening, Patients will be enrolled if they satisfy inclusion and exclusion criteria.  The patients will be assessed clinically at baseline and every two weeks during the treatment period. (i.e., 0, 2nd, 4th, 6th, 8th, 10th and 12th weeks). The subjective and objective clinical observations will be recorded in the follow-up sheet. The total duration of treatment will be 12 weeks. Laboratory parameters for safety assessment will be conducted at baseline and on completion of the protocol therapy (i.e., 0 and 12th weeks).

Itrifal-e-Muqil-Mullaiyan

S. No

Ingredients

Botanical Names

Quantity

|1.

Muqil

Commiphora mukul (Hook ex stocks) Engl.

350gm

|2.

Turbud Safaid

Operculina turpethum L Silva Manso.

120gm

|3.

Post-e-Halela Zard

Terminalia chebula Retz.

90gm

|4.

Post-Halela Kabli

Terminalia chebula Retz.

90gm

|5.

Post-e-Balela

Terminalia bellerica Roxb

90gm

|6.

Halela Siyah

Terminalia Chebula Retz

90gm

|7.

Aamla

Emblica officinalis Gaertn.

90gm

|8.

Mastagi

Pistacia lentiscus Linn

50gm

|9.

Raughan-e-Badam Shireen

Or

Raughan Zard

Prunus Amygdalus Dulcis

150gm

|10.

Asal or Qand Safaid

Honey

3.5kg

|11.

Aab-e-Gandana

Allium ascalonium L.

Q.S.

Roghan e Babuna Qawi

S. No

Ingredients

Botanical Names

Quantity

|1.

Sumbul-ut-Teeb

Nardostachys jatamansi D.Don. DC.

12 g

|2.

Bisbasa

Myristica fragrans Houtt.

12 g

|3.

Heel khurd

Elettaria cardamomum Maton

12 g

|4.

Hamama

Amomum racemosum L.

12 g

|5.

Tukhm-e-Katan

Linum usitatissimum L.

12 g

|6.

Ikleel-ul-Malik

Trigonella uncata Boiss. & Noe Lassen

12 g

|7.

Babuna

Matricaria chamomilla L.

48 g

|8.

Aab

Water

12 times of all the ingredients

|9.

Roghan-e-Kunjad

Sesamum indicum L.

Equal to all ingredients

Comparator group

Habb –e-Suranjan

S. No

Ingredients

Botanical Names

Quantity

|1.

Suranjan

Colchicum luteum Baker.

1 part

|2.

Post e Halela Zard

Terminalia chebula Retz

1 part

|3.

Shahm e Hanzal

Citrullus colocynthis (L.) Schrad

1 part

|4.

Muqil

Commiphora mukul (Hook ex Stocks) Engl.

1 part

|5.

Trurbud

Operculina turpethum (L) Silva Manso.

1 part

Roghan e suranjan

S. No

Ingredients

Botanical Names

Quantity

|1.

Suranjan

Colchicum luteum Baker.

50 g

|2.

Aab e karafs

Apium graveolens L.

50 g

|3.

Chiraita

Swertia chirata Buch. Ham exWall

50 g

|4.

Roghan e zaitoon

Olea europaea L.

150 g

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

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

入选标准

  • Patients fulfilling the 2010 ACR-EULAR Rheumatoid Arthritis Classification Criteria.

排除标准

  • 1.Severe cases of RA (Stage III & IV) & diagnosed cases of ankylosing spondylosis/ Gout.
  • 2.Cases with systemic manifestation of Rheumatoid arthritis.
  • Abnormality in any investigation done at baseline (SGOT, SGPT and ALP, Sr Creatinine, B.
  • Urea would be considered abnormal if raised more than 2.5 times the normal value), also Patients with GFR less than 60 will be exclude from the study.
  • Patient with High grade fever.
  • Disorders requiring long term treatment.
  • Patient is on treatment for any illness related to Endocrine & metabolic disorders.
  • Pregnancy and lactation.
  • Drug addicts (Alcohol, drugs).

结局指标

主要结局

The safety and efficacy of Unani Pharmacopeial formulation Itrifal-e-Muqil Mullaiyan & Roghan e Babuna Qawi in comparison with Habb-e-Suranjan & Roghan e Suranjan in Waja ul Mafasil (Rheumatoid Arthritis) will be carried out on the basis of DAS28 Form

时间窗: At baseline and every two weeks during the treatment period. (i.e., 0, 2nd, 4th, 6th.8th, 10th and 12th weeks).

次要结局

  • Haematological and biochemical investigations for safety assessment i.e., Hemogram, LFT,KFT, Urine Examination: Routine & Microscopic.(At baseline and at the end of treatment. i.e., 0 and 12th week)

研究者

发起方
Central Council for Research in Unani Medicine CCRUM New Delhi
申办方类型
Research institution
责任方
Principal Investigator
主要研究者

Dr N Zaheer Ahmed

Central Council for Research in Unani Medicine (CCRUM)

研究点 (3)

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