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To evaluate the efficacy and safety of Longvida capsule in the patients suffering from knee osteoarthritis.

Evaluation of the efficacy and safety of Capsule Longvida® Optimized Curcumin in knee osteoarthritis: A randomized double-blind controlled clinical study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2015/07/006061
Enrollment
40
Registered
2015-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Health Condition 1: null- Patients suffering from knee osteoarthritis.

Interventions

Intervention1: Capsule Longvida: One 400 mg capsule once a day with water before meal orally for 90 days. Control Intervention1: Capsule Ibuprofen: One 400 mg capsule once a day with water before meal

Sponsors

Pharmanza Herbal PvtLtd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex, 40 to 60 years of age diagnosed with osteoarthritis of the knee based on the American College of Rheumatology (ACR)criteria and patient willing to comply with study procedures and requirements.

Exclusion criteria

Exclusion criteria: 1.Patients with congenital arthropathy, rheumatoid arthritis, active gout, other type of arthritis with/without inflammation e.g. septic , fibromyalgia or collagen vascular disease 2.Patients with known history of coagulopathies 3.Osteoarthritis of any other joint except knee 4.Patients with history of major trauma or surgery in the knee joint 5.Patients with uncontrolled diabetes and hypertension 6.Body mass index (BMI) >40 kg/m2. 7.Patients with any severe cardiac, renal and hepatic disease 8.Pregnant and lactating women 9.Patients who participated in any clinical trial within 30 days before enrollment into the study

Design outcomes

Primary

MeasureTime frame
The primary outcomes of the study will be measured in terms of clinical signs by Local examination, Goniometry, WOMAC score and Visual analogue scale. Timepoint: After every 15 days

Secondary

MeasureTime frame
The secondary outcome will be measured by biochemical profiling of Inflammatory and degenerative markers.Timepoint: Inflammatory marker - Day0, Day7 and day 90 Degenerative marker - Day 0 and Day 90

Countries

India

Contacts

Public ContactDr Supriya Bhalerao

Interactive Research School for Health Affairs Bharati Vidyapeeth Deemed University

supriya.bhalerao@gmail.com9869555272

Outcome results

None listed

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