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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01239524
Other study ID # R06075
Secondary ID
Status Completed
Phase Phase 3
First received November 10, 2010
Last updated November 10, 2010

Study information

Verified date November 2010
Source Tampere University Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Ethics Committee
Study type Interventional

Clinical Trial Summary

Breast reconstruction with a pedicled myocutaneous latissimus dorsi (LD) flap is a widely used reconstruction method. It is controversial if surgical denervation by transecting the thoracodorsal nerve should be performed or not. It is assumed that after denervation the latissimus dorsi muscle will significantly atrophy and lose volume. On the other hand discomforting signs and symptoms from muscle contraction are believed to be prevented if flap is denervated. The aim of the study was prospectively evaluate the influence of LD-flap innervation on the functional and aesthetic outcome of delayed breast reconstruction, and to compare the change in muscle structure in breast MRI and histopathology.


Recruitment information / eligibility

Status Completed
Enrollment 28
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Female
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- delayed LD-flap breast reconstruction, no recurrent disease observed

Exclusion Criteria:

- recurrent cancer, partial resection of the breast

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Significance of Latissimus Dorsi Flap Innervation in Delayed Breast Reconstruction

Intervention

Procedure:
denervation of thoracodorsal nerve or saving the nerve


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital