Skip to content

Risk Factors for Benign Breast Disease

Risk Factors for Benign Breast Disease in Young Adult Women. Case-control Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04127422
Enrollment
500
Registered
2019-10-15
Start date
2019-11-28
Completion date
2021-04-30
Last updated
2020-11-19

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

Conditions

Benign Breast Disease

Keywords

Benign breast disease, Fibrocystic disease

Brief summary

Benign diseases of the breast are common clinical conditions that affect young women. Complaints related to the breast often cause significant discomfort and mental stress. The following study will try to identify the risk factors that may be associated with symptomatic benign breast diseases. Identification of such factors may help preventing and / or treating these conditions.

Detailed description

Benign breast disease (BBD) is a common cause of hospital visit. In young adults, benign breast conditions surpass cancer as a cause of symptoms related to the breast. However, breast symptoms may be associated with significant distress and may impose diagnostic difficulties. Moreover, certain pathological entities of benign breast conditions are well known to increase the risk of breast cancer. Identification of modifiable risk factors associated with symptomatic breast disorders has several potential benefits. Modification of such factors may help decrease patients' distress, hospital visits and indirectly decrease the risk of cancer. the available data point to the possible association of several environmental factors with symptomatic BBD. Most of the available information points to an association of BBD with anthropometric features, growth pattern, family history of breast conditions and dietary consumption. Substantial evidence are however lacking and further studies are strongly required to better characterize the risk factors of the condition. In this study, the investigators will systematically collect epidemiological, developmental and clinical data in young patients presenting with breast complaints. The association with disease incidence, pattern and histology will be examined.

Interventions

None listed

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 39 Years
Healthy volunteers
Yes

Inclusion criteria

* adult females with current symptoms related to the breast.

Exclusion criteria

* Current or past malignancy of the breast. * Discrete breast mass that necessitate work-up to exclude cancer. * Current psychiatric morbidity. * Persons unwilling to participate.

Design outcomes

Primary

MeasureTime frameDescription
Relative risk of benign breast disease associated with obesity.This outcome will be assessed at baseline (the first hospital visit).For the study and control groups, body mass index will be calculated as the weight (Kg) to square height (m) ratio.
Relative risk of benign breast disease associated with soda beverage consumption.This outcome will be assessed at baseline (the first hospital visit).for the study and control groups, the participant will be asked about soda beverage consumption in the last 30 days. never consumed is scored 0 (lowest score). Three or more times a day is scored 9 (highest score).
Relative risk of benign breast disease associated with caffeine beverages consumption.This outcome will be assessed at baseline (the first hospital visit).for the study and control groups, the participant will be asked about caffeine beverage consumption in the last 30 days. never consumed is scored 0 (lowest score). Three or more times a day is scored 9 (highest score).
Relative risk of benign breast disease associated with parity.This outcome will be assessed at baseline (the first hospital visit).for the study and control groups, the participant will be asked about her parity. response will be either nullipara, primipara, multipara or grand multipara ( 5 or more births).

Other

MeasureTime frameDescription
Relative risk of benign breast disease associated with hormonal contraception.This outcome will be assessed at baseline (the first hospital visit).for the study and control group, the participant will be asked about current hormonal contraception use.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026