A Clinical Study to Evaluate the Effectiveness of Swayambhuva Guggul Tablets Along with Prasarini Taila Nasya Therapy in Reducing Pain, Stiffness, and Restricted Shoulder Movement in Patients with Frozen Shoulder (Avabahuka

Evaluation of Efficacy of Swayambhuva Guggul Along With Prasarini Taila Nasya In The Management Of AVABAHUKA(FROZEN SHOULDER) - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/06/111832

Enrollment

Registered

2026-06-03

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-22

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

Conditions

Health Condition 1: M750- Adhesive capsulitis of shoulder

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1 Participants have classical signs & symptoms of Avabahuka 2 Participants suitable for Nasya Karma 3 Participants willing to sign written consent form for participation in the study

Exclusion criteria

Exclusion criteria: 1 Pregnant & lactating women 2 Dislocation and fracture affecting the shoulder joint 3 Participants with any disorders which interfere with the line of treatment of Avabahuka like OA etc

Design outcomes

Primary

Measure	Time frame
It is expected that at the end of study, scholar will be able to evaluate the efficacy of Swayambhuva Guggul Along With Prasarini Taila Nasya In The Management Of AVABAHUKA (FROZEN SHOULDER)Timepoint: 18 months	—

Secondary

Measure	Time frame
The secondary outcome of the study will include assessment of tenderness around the shoulder joint improvement in muscle strength & enhancement in quality of life of the patients the study will also observe the safety & tolerability of the treatment regimen & record any adverse effects during the trial period Overall clinical improvement & patient satisfaction after completion of therapy will also be evaluatedTimepoint: 18	—

Measure

Time frame

The secondary outcome of the study will include assessment of tenderness around the shoulder joint improvement in muscle strength & enhancement in quality of life of the patients the study will also observe the safety & tolerability of the treatment regimen & record any adverse effects during the trial period Overall clinical improvement & patient satisfaction after completion of therapy will also be evaluatedTimepoint: 18

—

Countries

India

Contacts

Public ContactDr Amit sharma

Pt khushilal sharma govt autonomous ayurveda college and institute

drvivek.sharma13@gmail.com8770672790

Outcome results