A clinical trial to study the effect of Pankajakasthuri Orthoherb Tablet in patients with pain, swelling and stiffness of joints.

An open clinical trial for the assessment of efficacy of Pankajakasthuri Orthoherb Tablet in patients with osteoarthritis.

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/02/012189

Enrollment

500

Registered

2018-02-27

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: M158- Other polyosteoarthritis Health Condition 2: M159- Polyosteoarthritis, unspecified Health Condition 3: null- The Patients with pain in joints visiting PANKAJAKASTHURI AYURVEDA MEDICAL COLLEGE OUT PATIENT DEPARATMENTS for consultation.

Interventions

Intervention1: PANKAJAKASTHURI ORTHOHERB TABLET-500mg: DOSE:TWO tablets ROUTE OF ADMINISTRATION:ORAL FREQUENCY:TWO TIMES PER DAY BEFORE FOOD TIME:FOR SIX MONTHS Control Intervention1: NOT APPLICABLE:

Eligibility

Inclusion criteria

Inclusion criteria: Classical Signs and Symptoms of Osteoarthritis - Pain during movement and weight bearing, Swelling, Stiffness. Also fulfilling the classical criteria of Sandhigatavata mentioned in Ayurvedic texts- Shoola i.e. Akunchana prasarana vedana, Shotha and Sthambha.

Exclusion criteria

Exclusion criteria: Secondary Arthritic conditons, Fractures, Ligament tear, Dislocation, Osteomyelitis, SLE, Tumors Bone density disorders, Anatomical joint deformities, NSAID/Analgesic/steroid treatment for Osteoarthritis, Patients who have undergone major surgery in the affected joint.

Design outcomes

Primary

Measure	Time frame
More than 80% of participants had 100% relief Assessment criteria was based on the grading of following parameters PAIN STIFFNESS TENDERNESS SWELLING. Timepoint: SPECIFIC TIME FOR ASSESSING PRIMARY OUTCOME : 6 MONTHS	—

Secondary

Measure	Time frame
An average of 60% of participants got MODERATE to CONSIDERABLE relief of symptoms. Assessment criteria was based on the grading of following parameters PAIN STIFFNESS TENDERNESS SWELLINGTimepoint: SPECIFIC TIME FOR ASSESSING SECONDARY OUTCOME : 4 MONTHS;More than 50% of participants got relief of symptoms ranging from MILD to MODERATE. Assessment criteria was based on the grading of following parameters PAIN STIFFNESS TENDERNESS SWELLING Timepoint: SPECIFIC TIME FOR ASSESSING SECONDARY OUTCOME : 2 MONTHS	—

Measure

Time frame

An average of 60% of participants got MODERATE to CONSIDERABLE relief of symptoms. Assessment criteria was based on the grading of following parameters PAIN STIFFNESS TENDERNESS SWELLINGTimepoint: SPECIFIC TIME FOR ASSESSING SECONDARY OUTCOME : 4 MONTHS;More than 50% of participants got relief of symptoms ranging from MILD to MODERATE. Assessment criteria was based on the grading of following parameters PAIN STIFFNESS TENDERNESS SWELLING Timepoint: SPECIFIC TIME FOR ASSESSING SECONDARY OUTCOME : 2 MONTHS

—

Countries

India

Contacts

Public ContactDrARUNPRATAP

Pankajakasthuri Ayurveda Medical College and Post Graduate Centre

dr.sreejith.satheesan@gmail.com9447791353

Outcome results

None listed

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