Efficacy of Ethnic Marma Therapy and Wet Cupping Therapy in Grivasandhigata Vata w.s.r. to Cervical Spondylosis

Efficacy of Ethnic Marma Therapy and Wet Cupping Therapy in Grivasandhigata Vata w.s.r. to Cervical Spondylosis An open Labelled A Randomised Comparative Clinical Trial - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/083716

Enrollment

Registered

2025-03-28

Start date

Unknown

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

Health Condition 1: M472- Other spondylosis with radiculopathy Health Condition 2: M488- Other specified spondylopathies

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Diagnosed patients of Grivasandhi gate vats (cervical spondylosis) within the age group 20-60 years will be enrolled irrespective irrespective of sex , religion, occupation , socioeconomic status etc. 2.Patients who who are compulsory with Grivasandhi shoola ( cervical pain ) & Grivasandhi Stambha ( stiffness in cervical region). 3. Patients including Grivasandhi shoola & Grivasandhi Stambha & none of Grivasandhi shopha & Prasaran Akunchana Pavritti

Exclusion criteria

Exclusion criteria: 1. Age below 20 years and above 60 years. 2. Patients with uncontrolled diabetes (RBS greater than 140mg/dl) and uncontrolled hypertension (BP greater than 160/90mmHg) 3. Tuberculosis of cervical spine & malignancy. 4. Patients with cervical rib, Fracture of Cervical Spine. 5. Other diseases like cardiac diseases, renal diseases and endocrine diseases, and severe Anaemia and immunosuppressive disorders, Serology Positive patients. 6. Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
1.Relief in pain and stiffness of Cervical Spondylosis. 2.Painless increased Angle to of the Movement ( AOM).Timepoint: 4 weeks	—

Secondary

Measure	Time frame
Cost effective Time saving Minimum facilities required Minimize side effects Non pharmacologicalTimepoint: 4 weeks	—

Countries

India

Contacts

Public ContactDr P B JOSHI

Institute of Teaching and Research in Ayurveda

pbj@itra.edu.in9427226504

Outcome results