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The effect of interferon alpha 2b on the treatment of basal cells cancer

A clinical trial on clinical response and complications of treatment with interferon alpha 2b in patients with basal cell carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017093017756N30
Enrollment
20
Registered
2017-10-01
Start date
2017-03-21
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

basal cell carcinoma. Malignant neoplasm of skin, unspecified

Interventions

The treatment involves subcutaneous administration of three million unite interferon alpha 2b ampule at a dose of 0.15 cubic centimeters per lesion three times a week for three successive weeks..
Treatment - Drugs
The treatment involves subcutaneous administration of three million unite interferon alpha 2b ampule at a dose of 0.15 cubic centimeters per lesion three times a week for three successive weeks.

Sponsors

Vice-chancellery for Research and Technology, Mashhad University of Medicla Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Informed written consent for participation; definitive diagnosis of basal cell carcinoma of skin in pathology; and age 18 years old or above. Exclusion criteria: Morphea-like basal cell carcinoma of skin; nodulo-ulcerative basal cell carcinoma; pregnancy and breast-feeding; previous history of severe complications with interferon alpha 2b; no intent to complete the treatment course; no intent to complete the follow-up period; previous history of cardiovascular disease; previous history of thromboembolic disease; local radiotherapy on the target region; previous history of arsenic exposure; and immune insufficiency.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical response. Timepoint: Every two months. Method of measurement: Physical examination.

Secondary

MeasureTime frame
Neutropenia. Timepoint: on a weekly basis. Method of measurement: Complete blood count.;Headache. Timepoint: on a weekly basis. Method of measurement: Medical history.;Fatigue. Timepoint: on a weekly basis. Method of measurement: Medical history.;Pathologic response. Timepoint: Two months after completion of treatment. Method of measurement: Biopsy.;Fever. Timepoint: on a weekly basis. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mehdi Razmara Farzaghi

Mashhad University of Medical Sciences

RazmaraM941@mums.ac.ir+98 51 3842 6936

Outcome results

None listed

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