Surgery of non-palpable benign lesion with skin-marking

Comparison of the correctness of the excised lesions (with pathology and sonography) in patients with a non-palpable benign breast lesion under the guidance of us-guided skin-marking and lesion local coordinates or guide-wire insertion

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20100706004329N8

Enrollment

Registered

2019-04-06

Start date

2019-04-09

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

Benign breast lesions. Disorder of breast, unspecified

Interventions

Intervention 1: Intervention group: Skin-marking of benign breast lesions with a pen under the guidance of ultrasonography. Intervention 2: Control group: Marking the lesion with guide-wire insertion

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Benign breast lesion Non-palpable lesion

Exclusion criteria

Exclusion criteria: Malignancy in the breast

Design outcomes

Primary

Measure	Time frame
The correctness of the excised lesion. Timepoint: After surgery. Method of measurement: With pathology and sonography.	—

Secondary

Measure	Time frame
Time of surgery. Timepoint: During surgery. Method of measurement: Measuring time with clock in minutes.;Wight of excised specimen. Timepoint: After surgery. Method of measurement: Measuring weight with digital weighting device in grams.;The convenience of Surgeon. Timepoint: After surgery. Method of measurement: Questionnaire (Likert scale).;The convenience of radiologist. Timepoint: After radiology. Method of measurement: Questionnaire (Likert scale).	—

Measure

Time frame

Time of surgery. Timepoint: During surgery. Method of measurement: Measuring time with clock in minutes.;Wight of excised specimen. Timepoint: After surgery. Method of measurement: Measuring weight with digital weighting device in grams.;The convenience of Surgeon. Timepoint: After surgery. Method of measurement: Questionnaire (Likert scale).;The convenience of radiologist. Timepoint: After radiology. Method of measurement: Questionnaire (Likert scale).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSadaf Alipour

Tehran University of Medical Sciences

salipour@sina.tums.ac.ir+98 21 7788 3283

Outcome results

None listed

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