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Effect of LANCONONE in Weight-bearing Joint Pain

Not Applicable
Completed
Conditions
Osteo Arthritis Knee
Interventions
Dietary Supplement: Lanconone®
Dietary Supplement: Methyl crystalline cellulose
Registration Number
NCT03658369
Lead Sponsor
Vedic Lifesciences Pvt. Ltd.
Brief Summary

The current study has been designed to primarily assess the effect of Lanconone® in comparison to placebo on pain in weight bearing joints.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria
  1. BMI ≥ 25 and ≤ 29.9 kg/m2.
  2. With unilateral or bilateral OA of the knee for at least greater than 3 months, as presented by pain in the knee at least for last 3 months.
  3. Post-menopausal females (LMP at least 12 months prior to the screening).
Exclusion Criteria
  1. History of osteoarthritis for more than 3 years.
  2. Systolic Blood Pressure ≥140 mm Hg and Diastolic Blood Pressure ≥ 90 mm Hg
  3. FBS>140 mg/dl.
  4. Smokers or chronic alcoholics.
  5. Participants planning to travel in the next 56 days or engage in any non-routine activity that is likely to strain the knees.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Lanconone®Lanconone®Lanconone®: 2 Capsules once a day after breakfast
Methyl Crystalline CelluloseMethyl crystalline cellulose2 Capsules once a day after breakfast
Primary Outcome Measures
NameTimeMethod
WOMAC (Western Ontario and McMaster universities Osteoarthritis Index) pain score56 days

Change in pain score.The score ranges from 0-5, wherein 0 indicates no pain and 5 indicates extreme pain.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

K.K Medical Centre

🇮🇳

Mumbai, Maharashtra, India

Siddhant Clinic

🇮🇳

Mumbai, Maharashtra, India

Ayush Nursing Home

🇮🇳

Mumbai, Maharashtra, India

Dinanath Nursing Home

🇮🇳

Mumbai, Maharashtra, India

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