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TO SEE THE EFFECT OF PATRA PINDA SWEDANA AND PARISHEKA IN AVABAHUKA

A COMPARATIVE CLINICAL STUDY OF PATRA PINDA SWEDANA AND PARISHEKA IN AVABAHUKA

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/06/054254
Enrollment
40
Registered
2023-06-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

None listed

Sponsors

Patanjali Bhartiya ayurvigyan evum anusandhan sansthan haridwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.patient fit for patra pinda swedana and parisheka. 2.patient with classical features of Avabahuka. 3.subjects with chronicity of disease pertaining from 3 months to 3 years. 4.patient with radiological findings of frozen shoulder. 5.post traumatic shoulder injuries. 6.shoulder joint arthritis.

Exclusion criteria

Exclusion criteria: 1.patient who are unfit for patra pinda swedana and parisheka. 2.Autoimmune disorders like SLE, RA etc. 3.Respiratory disorders like bronchial asthma, allergic bronchitis etc. 4.Uncontrolled metabolic disorders like diabetes mellitus. 5.Pregnant and lactating mothers. 6.Critical illness like cardiac disease, carcinoma , tuberculosis, HIV, neurological disorders.

Design outcomes

Primary

MeasureTime frame
Subjective parameters: 1.Sandhi shoola (joint pain) 2.Sandhi shosha (wasting of muscles) 3.sandhi graha(stiffness of joint) objective parameters: 1.Localized swelling on palpation 2.Tenderness 3.Movement restrictedTimepoint: 7,30 days

Secondary

MeasureTime frame
objective parameters: 1.Localized swelling on palpation 2.Tenderness 3.Movement restrictedTimepoint: 7,30 days

Countries

India

Contacts

Public ContactRuchi juyal

Patanjali Bhartiya aayurvigyan evum anusandhan sansthan

ketanmahajan82@gmail.com8979793731

Outcome results

None listed

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