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Nimba Kshar Application In Fissure In Ano

A Randomized Controlled Clinical study To Evaluate The Efficacy Of NimbaKshar Pratisaran In Parikartika With Special Reference To Fissure In Ano

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/10/021813
Enrollment
60
Registered
2019-10-29
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: O- Medical and Surgical

Interventions

Intervention1: nimbakshar (ointment base): 1gm for local application once a day upto 21 days over the fissure site Control Intervention1: jatyadi ghrut: 1gm for local application once a day upto 21 da

Sponsors

Department of shalya tantra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patient who are having classical sign symptoms of parikartika like constipation ,perianal itching, anal pain, sphincter spasm, burning sensation ,anal canal and per rectal bleeding Both acute and chronic fissure in ano will be taken Patient having fissure in ano from more than 6 week duration will be taken as chronic fissure Patient willing to participate in clinical trial/study with written consent

Exclusion criteria

Exclusion criteria: Patients with other systemic illness like uncontrolled Diabetes mellitus, Hypertension, malignancy, HBsAg and Retrovirus positive patients. Patient diagnosed with internal piles, Patient diagnosed with fistula in ano Diagnosed case of crohnâ??s disease Infective and Neoplastic conditions of rectum, Rectal prolapse,will be excluded. Pelvic pathology and Pregnancy. Patient not willing to participate in the clinical trial/study or written consent

Design outcomes

Primary

MeasureTime frame
reduction in sign and symptoms of fissure in ano like burning sensation painful defecation and per rectal bleeding and constipationTimepoint: 21 days

Secondary

MeasureTime frame
changes in visual analogue scale as per reduction in intensity of patients conditionTimepoint: 21 days

Countries

India

Contacts

Public Contactyogesh sharma

A.S.S. Ayurved college nashik

drsantoshsp@gmail.com

Outcome results

None listed

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