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Effect of Gomutra Arka in the Management of Psoriasis

Comparative Clinical Evaluation of Gomutra Arka & Virechanottar Gomutra Arka in the Management of Kitibha (Psoriasis) w.s.r. to Gut Microbiota Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029403
Enrollment
100
Registered
2020-11-26
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: L408- Other psoriasis

Interventions

Intervention1: Group 1: Gomutra Arka: The group 1, comprised of 50 patients will be administered Gomutra Arka orally 10ml twice a day for consecutive 2 months. Follow ups will be recorded monthly upto

Sponsors

KS Girhepunje
Lead Sponsor
Department of Kayachikitsa
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: i. Patient aged between 20 and 50 years ii. Diagnosed cases of Plaque Psoriasis iii. Patient willing to participate in this trial

Exclusion criteria

Exclusion criteria: i. Patients having age less than 20 yrs. and more than 50 yrs ii. Patients of guttate psoriasis, inverse psoriasis, erythrodermic and pustular psoriasis iii. Complicated cases of psoriasis like psoriatic arthritis and any other such type of complications iv. Severely ill patient with weight loss v. Patients having cardiac disease, renal disease and endocrine disorders will be excluded from the study vi. Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
1. Psoriasis Area Severity Index (PASI) 2. Effect on clinical features (Erythema, Scaling, Induration, Itching, Burning sensation)Timepoint: Before treatment (BT), After one month (F1), After two months (F2)and After three months of treatments (AT)

Secondary

MeasureTime frame
1. Gut microbiome analysis from stool culture 2. Complete blood count (CBC) 3. C- Reactive protein (CRP) 4. Erythrocyte sedimentation rate (ESR) 5. Liver function test (LFT) 6. Renal function test (RFT) 7. Lipid profile 8. Random blood sugar level (RBS)Timepoint: Before treatment (BT), After one month (F1), After two months (F2)and After three months of treatments (AT)

Countries

India

Contacts

Public ContactKS Girhepunje

Banaras Hindu University Varansi

singhopbhu@gmail.com9415818732

Outcome results

None listed

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