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Reduction Mammaplasty and Improved Quality of Life (MammaRed)

U

University Hospital Bratislava

Status

Completed

Conditions

Signs and Symptoms
Quality of Life
Macromastia

Treatments

Procedure: Reduction mammaplasty

Study type

Observational

Funder types

Other

Identifiers

NCT02769559
UHB/005/2015/MB

Details and patient eligibility

About

The data gathered here will be used to evaluate the efficacy and safety of the mammary reduction in patients with macromastia.

Full description

The data was gathered using retrospective and follow-up prospective study of a group of patients, consisting of adult women that underwent a breast reduction surgery at the Clinic of Plastic, Reconstructive and Aesthetic Surgery Faculty of Comenius University and at the University Hospital in Bratislava, Ružinov, during the time period between 2000 until May 2014. The data concerning the quality of life of these patients was gathered by using the globally standardized questionnaire "Breast Q questionnaire©" with the separate software system evaluation tool "QScore©". The statistical analysis was conducted using GraphpadPrism program v. 6.01. The total number of respondents consisted of 52 people who were followed-up for up to 12 years.

Enrollment

52 patients

Sex

Female

Ages

18 to 63 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • above 18 years
  • macromastia on clinical examination
  • fulfilled Breast Q Questionnaire prior to surgery and after surgery
  • signed informed consent

Exclusion criteria

  • failed to sign informed consent
  • failed to fill the Breast Q Questionnaire
  • patients with altered mental status and behaviour
  • patients with concomitant breast disease, or with previous breast interventions as are radiotherapy, surgery, or breast cancer

Trial design

52 participants in 1 patient group

Patients with macromasty
Description:
Female adult patients with symptomatic macromasty selected for elective reduction surgery
Treatment:
Procedure: Reduction mammaplasty

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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