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Evaluation of Using Fat Injection to Improve Breast Look after Mastitis

Evaluation of the Outcomes of Local Fat Grafting on the elimination of Aesthetic Complications in the Breasts of Patients Recovered from Idiopathic Granulomatous Mastitis (IGM)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100706004329N14
Enrollment
7
Registered
2025-08-17
Start date
2025-08-27
Completion date
Unknown
Last updated
2025-08-19

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

Conditions

Idiopathic Granulomatous Mastitis. Inflammatory disorders of breast

Interventions

Intervention 1: Intervention group: In these patients, fat grafting is done according to the breast scars and deformities. Thereafter they are closely monitored to prevent complications and ensure fas

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Confirmed diagnosis of IGM based on histological examination of biopsy tissue Confirmed resolution of IGM based on clinical evidence and the opinion of the treating physician Presence of aesthetic complications (such as deformity, scarring, asymmetry, etc.) Consent to participate in the study

Exclusion criteria

Exclusion criteria: Recurrence of the disease during the study period Loss to follow-up Inability to maintain communication

Design outcomes

Primary

MeasureTime frame
Severity of Breast Deformity (patient assessment). Timepoint: Before intervention and after each intervention. Method of measurement: Patient Questionnaire.;Severity of Breast Deformity (Physician assessment). Timepoint: Before intervention and after each intervention. Method of measurement: Clinical Assessment Questionnaire.;Scar size. Timepoint: Before intervention and after each intervention. Method of measurement: Clinical Assessment Questionnaire.;Number of Scars. Timepoint: Before intervention and after each intervention. Method of measurement: Clinical Assessment Questionnaire.;Level of scar dimpling. Timepoint: Before intervention and after each intervention. Method of measurement: Clinical Assessment Questionnaire.;Extent of retraction. Timepoint: Before intervention and after each intervention. Method of measurement: Clinical Assessment Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Sadaf Alipour

Tehran University of Medical Sciences

salipour@Sina.tums.ac.ir+98 21777719922

Outcome results

None listed

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