A trial to study the comparison of matrabasti with sahachar taila and swadamstradi taila in gridhrasi

Randomized controlled clinical trial to study the comparative efficacy of matra basti with sahachar taila and swadamstradi taila in management of gridhrasi - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/10/074859

Enrollment

Registered

2024-10-07

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

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

Conditions

Health Condition 1: M544- Lumbago with sciatica

Interventions

Control Intervention1: 1.Matrabasti with Sahachar taila 2.Matrabasti with Swadamstradi taila: 1.Matrabasti with Sahachar taila 60 ml for 7 days 2.Matrabasti with Swadamstradi taila 60 ml for 7 days C

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient with age group 30-70 years 2.Diseases described in ayurvedic text as basti arha 3.Patients having minimum 3 signs and symptoms of gridhrasi i.e. sphikpurva katiprushtajanujanghapadam kramat,stambha,toda,graha,grudhravatchalan,gaurava

Exclusion criteria

Exclusion criteria: 1.Patients who are mentioned as basti-anarha 2.Auto immune diseases like SLE,Ankylosing Spondylosis 3.Having severe crippling deformity 4.Patients having Spinal deformities,severe taumatic injury to spinal cord and having unbearable pain 5.Kniwn cases of Pulmonary TB,cardiac diseases,HIV,HbsAg. 6.Patientsbelonging to age group below 20 and above 70 years

Design outcomes

Primary

Measure	Time frame
Comparative Efficacy of Matra basti with sahachar taila and swadamstradi taila in management og gridhrasiTimepoint: 7 days	—

Secondary

Measure	Time frame
Study adverse effects of sahachar taila and swadamstradi taila if anyTimepoint: 18 months	—

Countries

India

Contacts

Public ContactMayuri Bharatkumar Kumbhar

Tilak Ayurved Mahavidyalaya

ayurvedapune@gmail.com9823050402

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026