Satisfaction, Pain and Function Outcomes of Breast Reduction Patients

NCT ID: NCT05288530

Last Updated: 2022-03-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

35 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-10-31

Study Completion Date

2018-09-30

Brief Summary

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To explore the indications and benefits of breast reduction. The investigators suspect all of the patients in this population suffer from neck/back pain and limitations in function. The investigators also want to review the patients in this group to determine if the amount of breast tissue removed or previous breast size affects outcomes for these patients. Patients will then be contacted for outcome data and satisfaction information. Ultimately, this information may lead to improvements in management and education of patients with macromastia.

Detailed Description

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Conditions

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Macromastia Hypertrophy Breast

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

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Inclusion Criteria

* Females
* Ages 21-71 years-old
* Hypertropy of the breast
* Macromastia
* post-surgical intervention for macromastia or hypertrophy of the breast

Exclusion Criteria

* Males
* BMI\>40
* Hypertrophy of the breast but without surgical intervention
* Macromastia but without surgical intervention
Minimum Eligible Age

21 Years

Maximum Eligible Age

70 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Claytor Noone Plastic Surgery

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Brannon Claytor

Role: PRINCIPAL_INVESTIGATOR

Claytor Noone Plastic Surgery

Other Identifiers

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R17-3683B

Identifier Type: -

Identifier Source: org_study_id

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