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The evaluation of effects of Daflon tablet on hemorrhoids

The evaluation of effects of Daflon tablet on symptoms of hemorrhoids, its relapse and patients' duration of hospitalization

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210625051698N1
Enrollment
200
Registered
2021-07-06
Start date
2021-08-23
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

Hemorrhoids. Hemorrhoids and perianal venous thrombosis

Interventions

Intervention 1: Intervention group: Daflon group: After inclusion patients consume Daflon 500mg, which is produced Amin pharmaceutical company and comprise flavonoid agents by tablet each 12 hours (ev

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over the age of 18 years old who were diagnosed with grade 3 or 4 of hemorrhoids based on a surgeons' physical exam and history taking

Exclusion criteria

Exclusion criteria: Does not have a history of previous treatment of hemorrhoids. Does not have a history of consumption or allergy to Daflon tablet. Does not have a history of renal failure or electrolytes imbalance. Does not have a serious underlying disease, including immunodeficiency disease, hyperparathyroidism, complete heart block, addison's disease, intestinal disorders, or malignancies.

Design outcomes

Primary

MeasureTime frame
Duration of improvements of sign and symptoms. Timepoint: 4 weeks after inclusion. Method of measurement: Duration of times that takes for patients for their signs to get improved.;Severity of sign and symptoms. Timepoint: 4 weeks after inclusion. Method of measurement: The severity of symptoms are going to get reported by patients 4 weeks after inclusion based on visual Analogue scale.;Relapse of sign and symptoms. Timepoint: 4 weeks after inclusion. Method of measurement: In case of resolution of symptoms in 4 weeks, patients report relapse of their symptoms.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Karimian

Karaj University of Medical Sciences

Mohsenkarimian494@gmail.com+98 26 3255 8080

Outcome results

None listed

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