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Nipple-Areola Complex Sensitivity After the Section of Periareolar Dermis in Breast Reduction

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01789450
Enrollment
50
Registered
2013-02-12
Start date
2013-06-30
Completion date
2015-06-30
Last updated
2013-04-29

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

Conditions

Sensitivity of Nipple-areolar Complex

Keywords

sensitivity, section of periareolar dermis, breast reduction

Brief summary

The purpose of this study is to evaluate the feasibility and sensitivity of nipple-areolar complex (NAC) prospectively due to the section of the dermis after decortication (Schwartzmann's maneuver), in 50 patients undergoing breast reduction surgery.

Detailed description

Preservation of the dermis after decortication regions of the areola and periareolar is considered relevant by most plastic surgeons. In patients whose CAP should be mobilized through large distances in order to correct breast ptosis, or in cases of dense breasts where noted little slip of skin over the breast parenchyma, the periareolar dermis causes limitation on the mobility of the NAC. In clinical practice, there is a greater mobilization of NAC when making a careful section of the dermis after decortication. In contrast, the appearance of partial necrosis in these cases has become a rarity, as no case of total necrosis was observed. Given the technical benefit observed due to greater mobilization, there is no report in the literature about how behaves the sensitivity of the NAC in these cases. To evaluate the sensitivity of the NAC will be used Semmes-Weisnstein's monofilament. Each point will be obtained five measurements. The largest will be scorned and the lowest value. The final value of each point corresponds to an arithmetic mean of the three remaining values.

Interventions

PROCEDURESection of Periareolar Dermis in Breast Reduction.

Sponsors

Universidade Federal de Pernambuco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients who willingly seek the service requesting breast reduction or mastopexy; * Patients who after consultation with the surgeon who led the research presents realistic expectation, being safe with the possible outcome of the surgery; * Patients who undertake to comply with the protocol previously presented and discussed with them;

Exclusion criteria

* Patients with prior breast surgery; * Patients with body mass index (BMI) greater than 34.9; * Patients with severe anemia; * Patients with neurological disease; * Patients with impairment cardiovascular; * Metabolic diseases - diabetes; * Patients with autoimmune disease; * Menopausal patients * Patients with collagen disease; * Patients with psychiatric disorders.

Design outcomes

Primary

MeasureTime frameDescription
Nipple-Areola Complex (NAC) Sensitivity3 weeksTo evaluate the sensitivity of the NAC in breast reduction

Secondary

MeasureTime frameDescription
Nipple-Areola Complex (NAC) sensitivity6 weeksTo evaluate the sensitivity of the NAC in breast reduction

Other

MeasureTime frameDescription
Nipple-Areola Complex sensitivity12 monthsTo evaluate the sensitivity of the NAC in breast reduction

Countries

Brazil

Contacts

Primary ContactJairo Z Sá, surgeon
jairozacche@gmail.com81 34675717

Outcome results

None listed

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