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Comparson effects of vitamin E and Diclofenac gel on breast pain

Comparison effects of vitamin E and Diclofenac gel on breast pain in patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016061428464N1
Enrollment
60
Registered
2016-07-24
Start date
2016-07-31
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

Breast pain. Mastodynia

Interventions

Intervention 1: The case group: Tab vitamin E 400 mg, Daily, for two months, Orally. Intervention 2: Control Group: Diclofenac Gel 1%, amount of 0/25 gr, Twice a day, for two month.
Treatment - Drugs
The case group: Tab vitamin E 400 mg, Daily, for two months, Orally
Control Group: Diclofenac Gel 1%, amount of 0/25 gr, Twice a day, for two month

Sponsors

Islamic Republic Azad of Shahrrood University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: having breast pain for more than six month; Patients with substantial pain, its intensity by the physician (visual analog scale) is measured; Other diseases is rejected; infertility is rejected(woman 18_49 age) Exclusion criteria: existence underlying breast disease in examination or sonography if necessary or mammography if necessary; having systemic diseases affecting on breast pains; contrainndication of vitamin E use; contraindication of NSAIDs use includ asthma, Hives, cardiovascular disease, sever renal diease; last tree month of pregnancy and lactation; People who have done open-heart surgery; users of supplementry drugs, NSAID, sedatives, sexual hormonal drugs; addicts and people not trend to be treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The first day of intervention, 30 days after the intervention, 60 days after the intervention. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Digestive disorder, diarhea, Asthma, Hives, cardiovascular disorder, third month of pregnancy, lactation. Timepoint: The first day of intervention, 30 days after the intervention, 60 days after the intervention. Method of measurement: Questionnair.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Seyed Fatemeh Amirkhalili

Islamic Republic Azad of Ahahrood University

Dr.amirkhalili@yahoo.com+98 23 3223 1067

Outcome results

None listed

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