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A clinical study to compare combined effect of viddha karma plus agnikarma with only agnikarma by panchadhatu shalaka in the management of avabahuka

A randomized comparative clinical trial to evaluate combined efficacy of viddha karma plus agnikarma with only agnikarma by panchadhatu shalaka in avabahuka

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021686
Enrollment
62
Registered
2019-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: M20-M25- Other joint disorders

Interventions

Intervention1: viddha karma plus agnikarma: Group A will be treated with Viddha Karma With 26 Gauze Needle Plus Agnikarma With Panchadhatu Shalaka in 3 settings with a gap of 7 days Control Interventi

Sponsors

PDEAs college of ayurved and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Typical Clinical features of avabahuk- stiffness, pain, restricted movement of arm, progressive loss of passive movement(PROM) and active range of movement(AROM)

Exclusion criteria

Exclusion criteria: known case of: Seropositive, Shoulder joint dislocation, Fracture, Rotatory cuff injury, Pregnancy

Design outcomes

Primary

MeasureTime frame
To compare the combined effect of Viddha karma plus Agnikarma with only Agnikarma by Panchadhatu Shalaka in 3 settings with gap of 7 days in the management of pain and stiffness in avabahuk on the basis of visual analogue scale and goniometer measurements.Timepoint: Difference in pain and stiffness will be obseved on 0,7,14 days—

Secondary

MeasureTime frame
To study adverse effect, if any.Timepoint: Difference in pain and stiffness will be observed on 0,7,14 days—

Countries

India

Contacts

Public ContactRutuja Ravindra Chavan

PDEAs college of ayurved and research centre

dr.madhavibanarase209@gmail.com9423207569

Outcome results

None listed

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