Results of reduction mammoplasty in two different pedicle surgical methods

Not Applicable

Recruiting

• Conditions: Reduction Mammoplasty.; Encounter for cosmetic surgery; Z41.1

• Registration Number: IRCT20230425057988N1
• Lead Sponsor: Iran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 June 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 32

Inclusion Criteria

Candidates for reduction mammoplasty
Women between 30 and 60 years old
Obtaining informed consent from patients

Exclusion Criteria

Patients who have already had breast surgery
Patients with underlying or neurological diseases
Patients with breast cancer

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
????? ??????. Timepoint: Before surgery and after surgery in the first, third and sixth month. Method of measurement: Using monofilament kit and tow point discrimination test method. In the monofilament method, this sensory test is performed by an evaluator in a standard way. Seven points on the chest are tested. These areas include one point in each quadrant (points 1 to 4), one point on the upper pole of the areola (point 5), one point on the lower pole of the areola (point 6), and one point on the nipple (point 7).

Secondary Outcome Measures

Name	Time	Method
Scar status. Timepoint: One, three and six months after surgery. Method of measurement: Observing the absence of infection or swelling and redness at the scar site.;Blood supply status. Timepoint: One, three and six months after surgery. Method of measurement: Observing the condition of blood supply and lack of tissue necrosis and change of skin color to indigo or dark nipple based on clinic clinical examinations.