Clinical Study To Compare Ashwagandhadi Granules Alone and Ashwagandhadi Granules With Cupping Therapy In Neck Pain

An Open Labelled Randomised Double Arm Clinical Study To Evaluate The Efficacy Of Ashwagandhadi Granules With and Without Cupping Therapy In The Management Of Manyastambh W.S.R. to Cervical Spondylosis - nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/02/103827

Enrollment

Registered

2026-02-13

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

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

Conditions

Health Condition 1: M479- Spondylosis, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients between ages of 18-60 years. 2.Patients having classical signs and symptoms of manyastambha. (cervical spondylosis) with or without radiological changes.

Exclusion criteria

Exclusion criteria: 1.Patient below the age of 18 and above age 60 years will be excluded in this study. 2.Known cases of trauma of neck, local wound and infection over neck, cervical rib syndrome, any spinal cord disorders other than cervical spondylosis , compress cord , canal stenosis. Known cases of shoulder and elbow musculoskeletal problems, fracture of spine and upper limb. 3.Patients with cervical spine diseases who are indicated for surgical intervention will be excluded from the study. 4.Severe anemia ( hb below 8) , bleeding disorders, hypotension. 5.Pregnant and lactating women.

Design outcomes

Primary

Measure	Time frame
1.To study the efficacy of Ashwagandhadi Granules with and without Cupping Threapy On The Basis Of Subjective Parameters From Baseline To end of The Study. 2.To reduce the pain by VAS (1 to 10) 3.To Reduce pain By NDITimepoint: Subjective Parameters:0,30,60th day VAS :0,15,30,45,60th Day NDI :0,30,60th Day	—

Secondary

Measure	Time frame
1.To Improve Range Of Motion by Goniometer. 2.To Iimprove quality of life by SF 36 Questionnaire .Timepoint: ROM : 0,15,30,45,60 th Day QOL : 0,30,60th Day	—

Countries

India

Contacts

Public ContactDr Riddhi V Varan

Parul Institute of Ayurved and research

drshivangi1989@gmail.com9981411478

Outcome results