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Evaluation of the efficacy of rectal preparation from Hemoheal® Cream in patients with Hemorrhoid

Evaluation of the efficacy of rectal preparation from Hemoheal® Cream on number of excretion daily and rate of rectal bleeding in patients with Hemorrhoid

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017091335460N1
Enrollment
40
Registered
2017-09-13
Start date
2017-10-12
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Hemorrohiod. Unspecified haemorrhoids with other complications

Interventions

Intervention 1: Intervention: Topical use of thin-layer Hemoheal cream twice a day for a month. Intervention 2: Control: Topical use of thin-layer eucerin base cream twice a day for a month.
Treatment - Drugs
Placebo
Intervention: Topical use of thin-layer Hemoheal cream twice a day for a month
Control: Topical use of thin-layer eucerin base cream twice a day for a month

Sponsors

Vice Chancellor for Research, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age>18 Patients who sign the testimonials and cooperate during the study Patients who their diseases are confirmed by complete medical evaluation including colonoscopy, pathology and laboratory data Only patients with mild to moderate hemorrhoids can be included in this study Patients who were not cured with Hemoheal cream during the last month

Exclusion criteria

Exclusion criteria: 4th-degree hemorrhoids Pregnant patients and nursing mothers Patients who have to use other drugs that interference with this medication Previous history of anorectal surgery Patients who are suffering from other diseases in addition to hemorrhoids, such as apparent coagulation abnormalities or kidney impairment accompanied with colorectal diseases such as cancer, Crohn's disease, ulcerative colitis, anal fistula, anal fissure, proctitis or perineal skin inflammation Patients who are disposed to a serious health danger, such as severe cardiac, liver or renal diseases If significant side effects occur, the patient will be excluded from the study and followed to end of the study Patients with severe allergy to this plant (dermatitis contact)

Design outcomes

Primary

MeasureTime frame
Number of excretion daily. Timepoint: Before using the drug; 2 weeks after using the drug-30 days after using the drugs. Method of measurement: Based on Hemorrohiod clinic questionary.;Rate of rectal bleeding. Timepoint: before using the drug; 2 weeks after using the drug-30 days after using the drugs. Method of measurement: based on Hemorrohiod clinic score.

Secondary

MeasureTime frame
Gastrointestinal disorders. Timepoint: Two weeks after using the drug; 30 days after using the drug. Method of measurement: Based on side effect questionary.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFateme Parvizi

Kermanshah University of Medical Sciences

parvizi_70@yahoo.com+98 833429920

Outcome results

None listed

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