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Effectiveness of BBETTER PsoriaUrja in Psoriasis

Efficacy and Safety of BBETTER PsoriaUrja in the Management of Psoriasis: A Randomized, Double-Blind, Placebo-Controlled Clinical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100854
Enrollment
70
Registered
2026-01-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

None listed

Interventions

Intervention1: BBETTER PsoriaUrja capsules 500 mg.: One capsule after breakfast and dinner (twice daily) with ambient temperature water for 8 weeks. Control Intervention1: Placebo Capsule (Identical t

Sponsors

MONKSAYS SUPERFOODS PVT. LYD.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Participants aged 18 to 65 years with mild to moderate plaque psoriasis (PASI score 5 to 15). 2. Presence of chronic stable psoriasis for at least 6 months. 3. Willingness to avoid additional psoriasis medications or phototherapy during the trial. 4. No recent use of systemic immunosuppressants (past 3 months). 5. Willingness to provide informed consent and comply with the study requirements.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Change in Psoriasis Area and Severity Index (PASI) scores from baseline.Timepoint: Baseline, Week 4, Week 8

Secondary

MeasureTime frame
Change in Transepidermal Water Loss (TEWL) scores from baseline.Timepoint: Baseline, Week 4, Week 8;Change in Dermatology Life Quality Index (DLQI) scores from baseline.Timepoint: Baseline, Week 4, Week 8;Change in Short Form-12 (SF-12) for Quality of Life score from baseline.Timepoint: Baseline, Week 4, Week 8;Change in Patient Global Assessment (PGA) score from baseline.Timepoint: Week 4, Week 8;Change in Inflammatory Biomarkers (IL-6, TNF-a, CRP) from baseline.Timepoint: Baseline, Week 8;Change in oxidative stress markers (MDA, SOD) from baseline.Timepoint: Baseline, Week 8;Change in laboratory values for liver parameters (serum alanine transaminase, aspartate transaminase, alkaline phosphatase, bilirubin) from baselineTimepoint: Baseline, Week 8;Change in laboratory values for kidney parameters (serum creatinine, blood urea nitrogen) from baseline.Timepoint: Baseline, Week 8;Change in Treatment-Emergent Adverse Events (TEAEs) from baseline.Timepoint: Baseline, Week 4, Week 8;Change in Treatment-Emergent Serious Adverse Events (TESAE) from baseline.Timepoint: Baseline, Week 4, Week 8

Countries

India

Contacts

Public ContactDr Revathi Vavilapalli

Government Medical College & Govt. General Hospital

drrevathivggh@gmail.com09912320517

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026