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Short - and medium-term efficacy and complications of areola incision biplane augmentation mammaplasty with different surface materials

A prospective, single-center, non-randomized clinical study: short - and medium-term efficacy and complications of biplanar augmentation mammification through areola incisions with different surface materials

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100041892
Enrollment
Unknown
Registered
2021-01-09
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-30

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

Conditions

Breast atrophy

Interventions

1:use smooth round implant
2:use textured anatomical implant

Sponsors

Guangdong Second Provincial General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Primary breast dysplasia; (2) Mammary gland dysplasia or non-development caused by lesions of mammary gland tissue (such as infection and trauma) before puberty; (3) Breast atrophy after birth and lactation; (4) The body is thin and the breast is atrophic after sudden weight loss; (5) The size of both sides of the breast is asymmetric, which can be corrected by augmentation mammoplasty; (6) The poor shape of the breast does not match the overall shape of the body; (7) Slightly saggy breasts; (8) Desire to increase breast volume during correction of breast ptosis.

Exclusion criteria

Exclusion criteria: (1) For patients with breast tissue inflammation or obvious infection near the surgical incision, surgery can be performed only after the inflammation is completely controlled; (2) Infected lesions in other parts of the body; (3) Combined immune system diseases; (4) Poor general conditions, poor control of cardiopulmonary dysfunction, and intolerance to surgery; (5) Pregnant women or those who become pregnant within one year after surgery.

Design outcomes

Primary

MeasureTime frame
Perioperative correlation index;visual analogue scale, VAS;Scar Cosmesis Assessment and Rating, SCAR;Evaluation of patient satisfaction;

Countries

China

Contacts

Public ContactSheng-Kang Luo

Guangdong Second Provincial General Hospital

luoshengkang63@hotmail.com+86 13719095959

Outcome results

None listed

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