Skip to content

Siravedh and trayodashanga guggulu in the management of Cervical pain with radiation

Therapeutic Impact of Siravedha and Tryodashang Guggulu in Cervical Radicular Pain w.s.r. to Vishwachi: A Three Arm Randomised Clinical Study - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100230
Enrollment
45
Registered
2026-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Health Condition 1: M501- Cervical disc disorder with radiculopathy

Interventions

Intervention1: Siravedha and orally Trayodashanga guggulu to be given: In one group we will be performing only siravyedha on 15 patients , in anathore we will be giving trayodashanga guggulu orally an

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age from 40- 60 year of age Patients present with symptoms of cervical radicular pain w.s.r. to Vishwachi. Patient fit for Siravedha. Diagnosed with clinical examination.

Exclusion criteria

Exclusion criteria: Severe Degenerative or Structural Conditions of cervical spine Hb less than 10 percentage Serological Positive Systemic Disorders & Bleeding Disorders Neurological Conditions. Cervical injury up to 6 months. Cardiovascular diseases Uncontrolled Diabetes Mellitus, Hypertension Thoracic outlet syndrome Localized Infections/Skin Conditions

Design outcomes

Primary

MeasureTime frame
Reduction in cervical radicular pain intensity, assessed by using the Visual Analogue Scale (VAS) and Neck Disability Index (NDI) from baseline to end of treatment and follow-up.Timepoint: Reduction in cervical radicular pain intensity, assessed by using the Visual Analogue Scale (VAS) and Neck Disability Index (NDI) from baseline on 1st day , on 11 th day and after 21 days during treatment .

Secondary

MeasureTime frame
Increase in cervical range of motion (ROM), measured by goniometric assessment. Improvement in quality of life, assessed using a standard tool (e.g., WHOQOL-BREF or SF-12)Timepoint: Improvement in cervical spine mobility. Sustained relief at follow-up intervals, indicating long-term efficacy. Patient-reported improvement in daily functional activities & quality of life. will be assessed after 21 days & every 15 days till one month post treatment

Countries

India

Contacts

Public ContactProf(Dr).Suman Sharma

National Institute of Ayurveda

sumanhp2006@gmail.com9418159666

Outcome results

None listed

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