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Dose-response relationship research of autologous fat transplantation in breast reconstruction after mastectomy

Dose-response relationship research of autologous fat transplantation in breast reconstruction after mastectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IND-17013888
Enrollment
Unknown
Registered
2017-12-13
Start date
2015-03-01
Completion date
Unknown
Last updated
2017-12-18

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

Conditions

Breast Cancer

Interventions

A-High dose :Inject 200-300ml (including 200ml ) autograft fat in one side of breasts each time
B-Low dose:Inject 200-300ml (including 100ml) autograft fat in one side of breasts each time

Sponsors

Plastic Surgery Hospital, CAMS
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. patients who have breast deformity after mastectomy; 2. loss of breast volume of more than 300 ml; 3. no recurrence of breast cancer within 2 years; 4. no chemical therapy within 6 months; 5. female; 6. Aged 20-55 years old; 7. sign surgical consent form; 8. involved into this trial within 24 months after it begins.

Exclusion criteria

Exclusion criteria: 1. patients with chronic diseases who are unsuitable for operations; 2. patients who are allergic to anesthetic drugs; 3. patients with acute diseases during treatment or those who with recurrence of breast cancer; 4. patients who do not sign surgical consent form.

Design outcomes

Primary

MeasureTime frame
Fat retention rate;

Secondary

MeasureTime frame
three party satisfaction survey;

Countries

China

Contacts

Public ContactFACHENG LI

Plastic Surgery Hospital, CAMS

drlfc@sina.com+86 13911116586

Outcome results

None listed

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