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Treatment of Constipation(Qabz) naturally with Safoof-i-Banafsha a unani remedy

A clinical study to evaluate the effect of Safoof-i-Banafsha in management of Daimi Qabz (Chronic Constipation) - A randomised double blind placebo controlled trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068794
Enrollment
40
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: K590- Constipation

Interventions

Intervention1: Safoof-i-Banafsha: After identification and authentication of the drug, Banafsha(viola odorata) will be finely powdered, sieved with No.80 mesh, mixed with equal quantity of Khand (Misr

Sponsors

Luqman Unani Medical College Hospital and Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Participants of either sex in the age group equal or more than 21years. 2.Patients meeting the "Rome IV diagnostic criteria for functional constipation" were included The criteria included experiencing two or more of the following: a. Straining during at least 25% of defecations b. Lumpy or hard stool in at least 25% of defecation. c. Sensation of incomplete evacuation for at least 25% of defecations d. Sensation of anorectal obstruction/blockage for at least 25% of defecations e. Manual maneuvers to facilitate at least 25% of defecations (e.g., digital evacuation, support of the pelvic floor) f. Fewer than three defecations per week 3.Loose stools are rarely present without the use of laxatives.

Exclusion criteria

Exclusion criteria: Patients using laxative medication (past 3days) and/or those on medications known to cause constipation (such as opioid analgesics, antidepressants, anticonvulsants). Individuals with a known case of megacolon/megarectum and obstructive cause of constipation. Cases with known HIV/AIDS, cancer, etc. Those with a known hypersensitivity to the study drug or any of its ingredients. Pregnant and lactating females. Individuals with Diabetes Mellitus.

Design outcomes

Primary

MeasureTime frame
Improvement in sign and symptoms of Daimi Qabz (Chronic constipation) by 1.VAS (Visual Analogue Scale) Straining at defecation Lumpy or hard stools Sensation of incomplete evacuation Sensation of anorectal blockage 2.Freuency of Bowel movement per day (0 to 2point scale) 3.Likert’s scale for manual maneuver. Timepoint: At baseline and every follow up and after completion of treatment

Secondary

MeasureTime frame
PAC-QOL QuestionnaireTimepoint: At baseline and after completion of treatment

Countries

India

Contacts

Public ContactDr Khan Ameer Kauser Khan

Luqman Unani Medical College Hospital And Research Centre

drmqkhan@yahoo.com9849438319

Outcome results

None listed

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