Skip to content

Comparing the efficacy of Calmax herbal and anti-hemorrhoid suppositories on symptoms of hemorrhoid patients

Comparing the efficacy of Calmax herbal and anti-hemorrhoid suppositories on symptoms of hemorrhoid patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080901001165N70
Enrollment
80
Registered
2023-01-17
Start date
2023-01-21
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Hemorrhoid. Hemorrhoids and perianal venous thrombosis

Interventions

Intervention 1: Intervention group: Calmex suppository (produced by Tabib-Daru Pharmaceutical Company, containing oak placenta extract from Quercus infectoria plant, essential oil from Myrtus communis

Sponsors

Bagheiat-allah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 18 to 60 years old A definite diagnosis of hemorrhoids by a specialist doctor Hemorrhoids with grade 1 and 2 severity The patient must have a written informed and free consent to participate in the study

Exclusion criteria

Exclusion criteria: Patients with thrombosed external hemorrhoids Patients with strangulated internal hemorrhoids Patients with anal fistula Patients with anal fissure Patients with anal abscess Pregnancy Patients with portal hypertension Patients with malignancy Patients with kidney failure Patients with grade 3 and 4 hemorrhoids Having a history of allergic reaction The occurrence of a severe allergic reaction

Design outcomes

Primary

MeasureTime frame
Rectal bleeding. Timepoint: Days 0 and 14. Method of measurement: Clinical examination.;Heaviness of the anus. Timepoint: Days 0 and 14. Method of measurement: Question from the patient.;Itching of the anus. Timepoint: Days 0 and 14. Method of measurement: Question from the patient.;Anus burning. Timepoint: Days 0 and 14. Method of measurement: Question from the patient.

Secondary

MeasureTime frame
Side effects. Timepoint: Days 0 and 14. Method of measurement: Question from the patient and clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFereshteh Dehdar

Bagheiat-allah University of Medical Sciences

dr.f.dehdar@gmail.com+98 21 8804 0060

Outcome results

None listed

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