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Efficacy Of Nimba Patra In The Management Of Sheetapitta(Urticaria)

Evaluation Of Efficacy Of Nimba-Patra(Azadirachta indica)In The Management Of Sheetapitta(Urticaria):Randomized Controlled Trial. - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111951
Enrollment
76
Registered
2026-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: L508- Other urticaria

Interventions

None listed

Sponsors

PMTS Ayurved College Shevgaon
Lead Sponsor
PMTS Ayurved College Shevgaon
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age and sex-18 to 60 years of either sex. 2. Patients with classical sign and symptoms of sheetapitta like a. Kotha b. Kandu c. Toda d. Daha

Exclusion criteria

Exclusion criteria: 1. Diabetes Mellitus 2. Hypertension 3. Tuberculosis 4. Use of systemic immuno-suppressive drugs, systemic corticosteroids, cytotoxic agents. 5. Use of antihistamines , systemic steroids or ayurvedic interventions for sheetapitta/urticaria within 2 weeks prior to baseline. 6. Presence of other primary dermatological disease like psoriasis,atopic dermatitis,scabiesthat may interfere with assessment of sheetapitta symptoms.

Design outcomes

Primary

MeasureTime frame
To Evaluate efficacy of Nimbpatra in sheetpitta.Timepoint: 7days

Secondary

MeasureTime frame
1. To review the literature of Nimb-patra from various ayurvedic samhitas. 2. To review sheetapitta according to ayurved & urticaria according to modern. 3. To evaluate efficacy of Navkarshik Guggul in sheetapitta. 4. To evaluate comparative efficacy of Nimb-patra with Navkarshik guggul in sheetapitta . 5. To observe any adverse effect of drug.Timepoint: 7days

Countries

India

Contacts

Public ContactDrSandeep Thaknath Shinde

PMTS Ayurved College Shevgaon

vd.sandeepshinde@gmail.com9405766631

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026