To see the effect of Trilawan Pashugandhadi churna orally and Lakshadi Oil locally in the management of Katigraha w.r.s. Lumbar Spondylosis.

“Randomized open controlled clinical study to evaluate the efficiency of ‘Trilawan Pashugandhadi Churna’ orally and ‘Lakshadi Tailam’ locally in the management of Katigraha w.s.r.to Lumber Spondylosis in the age group of 35 to 70 years ? - Yes

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064857

Enrollment

Registered

2024-03-27

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M471- Other spondylosis with myelopathy

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Age group 35- 70 years irrespective of caste religion socio-economic and educational status 2 The Roland and Morris disability questionnaire if RDQ score more than 5 3 Radiological degenerative changes in Lumbar Spine 4 Patient having sign and symptoms of Katigraha according to classics 5 Patient willing and able to participate in the study 6 Chronic low back pain more than three months

Exclusion criteria

Exclusion criteria: 1 History of any fracture of vertebral joints and surgical and diagnostic intervention with reference to affected joints will be excluded Gross disability in performing daily normal routine i.e. bedridden patient or confined to a wheelchair will be excluded. 3 Patient with co-morbidities such as gouty arthritis, rheumatoid arthritis or psoriatic arthritis and tubular arthritis 4 Patient with any deformity of Hip or back altering the gait and posture of the patient, ankylosing spondylitis, pelvic i inflammatory disorder 5 Severe alcoholic patient. 6 age group below 35 yrs and above 70 yrs 7 Degenerative disc disease may lead to spinal stenosis (narrowing of the spinal canal), vertebral instability

Design outcomes

Primary

Measure	Time frame
In present clinical trial the patient will be assessed based on the signs and symptoms mentioned described in the Ayurveda texts (A) SUBJECTIVE CRITERIA The parameters will be noted down before and after treatment 1 Katishul (Lumbar region) 2 Aakunchan Prasaran Shula (Pain on flexion and extension) 3 Graha (Stiffness) 4 Pindanashtava (Tenderness) 5 AnidraTimepoint: 0 7th 15th 22nd 29th 36th 45th 60th 75th 90th Days	—

Measure

Time frame

In present clinical trial the patient will be assessed based on the signs and symptoms mentioned described in the Ayurveda texts (A) SUBJECTIVE CRITERIA The parameters will be noted down before and after treatment 1 Katishul (Lumbar region) 2 Aakunchan Prasaran Shula (Pain on flexion and extension) 3 Graha (Stiffness) 4 Pindanashtava (Tenderness) 5 AnidraTimepoint: 0 7th 15th 22nd 29th 36th 45th 60th 75th 90th Days

—

Secondary

Measure	Time frame
OBJECTIVE CRITERIA 1 Roland & Morris Disability Questionnaire 2 VAS scaleTimepoint: 0 7th 15th 22nd 29th 36th 45th 60th 75th 90th Days	—

Countries

India

Contacts

Public ContactDr Subhash Bhikaji Jamdhade

Dayabhai Mavaji Majithiya Ayurved Mahavidyalaya Yavatmal

drsubhashjamdhade@gmail.com9822201196

Outcome results