Prospective Biomechanical Analysis of Donor-site Morbidity Following Microvascular Fibula Transplantation

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

27 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-09-30

Study Completion Date

2014-06-30

Brief Summary

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Pre- and postoperatively patients who underwent free fibula flap were examined regarding donor-site morbidity of the lower extremities.

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Detailed Description

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27 patients are examined before and after microsurgical fibula flap performed at the Department of Oral and Maxillofacial Surgery, University Medical Center Hamburg Eppendorf, Germany.

Conditions

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Postoperative Complications

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Fibula Explantation

surgical harvest of an osteomyocutaenous transplant consisting of a part of the fibula and surrounding soft tissues

Intervention Type PROCEDURE

Other Intervention Names

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Free fibula flap autologous fibula transfer

Eligibility Criteria

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Inclusion Criteria

* Planned continuity interrupting mandible resection
* Planned mandible reconstruction with free fibula flap
* Informed consent
* Procedure performed at University Medical Center Hamburg Eppendorf

Exclusion Criteria

* Preexisting pathology/disease of the lower limbs or back (angiologic, neurologic, orthopedic)
* Musculosceletal pain at the time of study enrollment

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes