Evaluate The Effect Of Dwitiya Baladi Yapana Basti With Trayodashang Guggulu Over Eranda Muladi Yapana Basti With Trayodashang Guggulu In Patients Having Katigraha (Lumbar Spondylosis)

A comparative clinical study to evaluate the efficacy of Dwitiya Baladi Yapana Basti with Trayodashang Guggulu over Eranda Muladi Yapana Basti with Trayodashang Guggulu in the management of Katigraha (Lumbar spondylosis) - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/073095

Enrollment

Registered

2024-08-29

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

Health Condition 1: M478- Other spondylosis

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients Of Any Gender Of Age Between 21-50 Years 2)Patients Having Classical Clinical Signs And Symptoms Of Katigraha (Lumbar Spondylosis)With Shool Stambh Gaurav 3)ODI Scale Scoring Between 5-24 That Is Mild To Moderate Cases 4)Abendeen LBP Scale More Than 40 5)Controlled Diabetes Mellitus Hypothyroidism Hypertension

Exclusion criteria

Exclusion criteria: 1)Patients Having Any Other Spinal Morbidity Like Spinal Tumor Any Other Deformities Of Lumbar Spine 2) Recent Lumbar Surgery Less Than 3 Years Or Implanted Instruments Or Prostheses 3)Chronic Inflammatory Metabolic Or Infective Pathogies That Is Ankylosing Spondylitis Rheumatoid Arthritis Psoriatic Arthritis Gouty Arthritis Potts Spine Malignancy And Or Metastasis In Bones 4)Patients Using NSAIDs And Or Corticosteroids On Regular Basis 5)Anorectal Conditions Like Haemorrhoids Anorectal Fistulae Anal Fissure Anal Mass Etc Those May Interfere With Basti Chikitsa 6) Pregnant Or Lactating Women 7)Any Other Systemic Illnesses Like IHD Epilepsy COPD Etc 8)Katigraha Due To Other Causes Like Malignant Disease Of The Pelvis

Design outcomes

Primary

Measure	Time frame
1)An improvement of about 30% in clinical symptoms of Katigraha in selected patients 2)An improvement of about 30% in range of motion of lower back in patients with Katigraha 3)An improvement of about 30% in quality of life in patients with Katigraha 4)Validation of the safety of ayurveda interventions proposed in Katigraha by assessing ADRs AEs if any Timepoint: Day 0 Day 8 Day 38	—

Secondary

Measure	Time frame
1)An improvement of about 30% in clinical symptoms of Katigraha in selected patients 2)An improvement of about 30% in range of motion of lower back in patients with Katigraha 3)An improvement of about 30% in quality of life in patients with Katigraha 4)Validation of the safety of ayurveda interventions proposed in Katigraha by assessing ADRs AEs if any Timepoint: Day 0 Day 8 Day 38	—

Countries

India

Contacts

Public ContactDr Amrish Dedge

All India Institute Of Ayurveda

dramrishaiia@gmail.com9025638650

Outcome results