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Effect of Unani medicine Habb-e-Bawaseer Damiya in Bleeding Piles

Clinical Validation of a Unani Pharmacopoeial formulation â?? Habb-e-Bawaseer Damiya in BawÄ?sÄ«r DÄ?miya (Bleeding Piles)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/10/016190
Enrollment
300
Registered
2018-10-29
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: null- BawÄ?sÄ«r DÄ?miya (Bleeding Piles) Health Condition 2: K648- Other hemorrhoids

Interventions

Intervention1: Habb-e-Bawaseer Damiya ( 259 mg): 1 tablet orally once daily with water one hour after meals for two weeks Control Intervention1: nil: nil

Sponsors

Central Council for Research in Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of any sex in the age group 19 to 65 years 2. Patients with a diagnosis of First and Second Degree Hemorrhoids presenting with any of the following symptoms: 3.Bleeding Per Rectum (JarayÄ?n al-Dam fiâ??l Maqâ??ad): bright-red, painless bleeding 4. Mucoid Anal/ Perianal Discharge (SayalÄ?n al-Maqâ??ad MukhÄ?tÄ«): mucus discharge 5. Pruritus Ani (Hikka al-Maqâ??ad) 6. Mucosal Prolapse (KhurÅ«j al-MukhÄ?tÄ«yya) with Spontaneous Reduction 7. Rectal/ Anal Pain (Wajaâ?? al-Maqâ??ad): on prolapse

Exclusion criteria

Exclusion criteria: 1. Third & Fourth Degree Haemorrhoids, anal fissure, anal fistula, IBD, Diabetes Mellitus 2. Known cases of other clinically significant co-morbid conditions (severe hepatic, renal, cardiovascular disorders, etc.) that in the opinion of the investigator could affect the efficacy and safety outcome of the study 3. Patients with laboratory values outside the normal limits or those with values considered abnormal in the opinion of the investigator 4. Known hypersensitivity to study drug or any of its ingredients 5. History of alcohol and drug abuse 6. Pregnant and Lactating Women

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of BawÄ?sÄ«r DÄ?miya (Bleeding Piles)Timepoint: 2 weeks

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessmentTimepoint: At baseline and after two weeks

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

ccrum507@rediffmail.com

Outcome results

None listed

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