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Treatment of Haemorrhoid (Bawaseer) with Unani Medicine Habb-e-Anjeer

Clinical Validation of Unani pharmacopoeial formulation Habb-e-Anjeer in Bawaseer (Haemorrhoids). - NILL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/08/092362
Enrollment
110
Registered
2025-08-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: K641- Second degree hemorrhoids

Interventions

Intervention1: Habb-e- Anjeer: 2 Pills (1 gm each) Twice a day With water after meal for 6 weeks Control Intervention1: Nil: Nil Control Intervention2: nil: nil

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of Internal Haemorrhoids presenting with any of the following symptoms: 1. Mucoid Anal and Perianal Discharge 2. Pruritus Ani (Hikka al-Maq ad) 3. Rectal and Anal Pain (Waja-al-Maq ad) 4. Rectal Bleeding

Exclusion criteria

Exclusion criteria: 1. Third & Fourth Degree Internal Haemorrhoids, 2. Severe Anaemia (Hb less than 8 g/dL) 3. Known cases of fistula and fissure in anal canal 4. Patient with rectal prolapse, polyp and abdominal mass. 5. Known cases of IBD & Bowel carcinoma. 6. Immuno-compromised clinical conditions such as diabetes mellitus type 2, HIV/AIDS, cancer, etc. 7. Known cases of other clinically significant co-morbid conditions (severe hepatic, renal, cardiovascular disorders, etc.) 8. Pregnancy and lactation

Design outcomes

Primary

MeasureTime frame
The efficacy of the study drug in the treatment of Bawaseer (Haemorrhoids) will be assessed on the basis of Haemorrhoidal Disease Symptom Score i.e., Pain, Itching, Bleeding, soiling, and prolapse as proposed by Nystr m et al (2010).Timepoint: At baseline and every two weeks. (i.e., 0, 2nd, 4th, and 6th week)

Secondary

MeasureTime frame
Haematological & biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline, first follow up and the end of treatment. (i.e., o, 2nd and 6th week)

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

javed.ghazal@gmail.com9811810454

Outcome results

None listed

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