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Reliability and Versatility of Supraclavicular Artery Flap in Reconstruction of Head and Neck Soft Tissue Defects

Reliability and Versatility of Supraclavicular Artery Flap in Reconstruction of Head and Neck Soft Tissue Defects

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05727150
Enrollment
20
Registered
2023-02-14
Start date
2023-02-28
Completion date
2024-01-31
Last updated
2023-02-14

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

Conditions

Reconstruction of Head Soft Tissue Defects, Reconstruction of Neck Soft Tissue Defects

Brief summary

This is a case series study conducted at plastic surgery department Sohag University including 20 patients The aim of this thesis is to evaluate reliability and versatility of Supraclavicular artery flap in the reconstruction of traumatic and non-traumatic defects of head and neck.With adequate documentation of functional, aesthetic outcome and patient satisfaction through; clinical examination , photographic documentation and doctor and patient satisfaction charts

Interventions

PROCEDUREReconstruction of Soft tissue defects of head and neck by Supraclavicular artery flap

Supraclavicular artery flap will be used in the reconstruction of traumatic and non-traumatic defects of head and neck.Flap harvesting and reconstruction will be performed under general anesthesia. The defect dimensions are measured and the superficial landmarks for the supraclavicular artery are drawn .The flap will be used as island flap, transposed or interpolated flap depending on the arc of rotation needed to achieve flap inset without tension and flap elevation proceeds from lateral to medial.The flap is rotated and inset into the defect

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients with head and neck soft tissue defect either traumatic or non-traumatic * Available healthy donor site

Exclusion criteria

* Trauma or conditions affecting donor site or with possible compromise of vascular pedicle. * Patients with a major uncontrollable medical illness, chronic heavy smokers.

Design outcomes

Primary

MeasureTime frameDescription
Flap Success6 month post-surgeryThe flap success will be measured by percentage of patients in which there is flap survival versus percentage of patient with flap necrosis
Flap complications6 months post-surgeryassessment of flap complication will be assessed by percentage of patients in which there is flap dehiscence , flap infection and flap necrosis
patients satisfaction as regard flap color match6 months post-surgerypatient satisfaction as will be assessed with questionnaire
patients satisfaction as regard flap texture match6 months post-surgerypatient satisfaction as will be assessed with questionnaire

Secondary

MeasureTime frameDescription
Possible flap lengths6 months post-surgeryThe achieved flap length will be measured in centimeters
Possible flap widths6 months post-surgeryThe achieved flap width will be measured in centimeters

Countries

Egypt

Contacts

Primary ContactAhmad A Albadry
ahmedahmed@med.sohag.edu.eg20111088856
Backup ContactKaram A Mohammed
karam.allam@med.sohag.edu.eg201021777543

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026