ClinicalTrials.Veeva

Menu

Prospective Diagnostic Study on Perforator Localization of Anterolateral Thigh Flap With Perforator Locator

Sun Yat-sen University logo

Sun Yat-sen University

Status

Completed

Conditions

Blood Vessel Perforation

Treatments

Device: perforator locator

Study type

Interventional

Funder types

Other

Identifiers

NCT05924984
SYSKY-2023-391-01

Details and patient eligibility

About

Oral and maxillofacial region is an important anatomical part of human body, responsible for chewing, swallowing, language, expression, breathing and other physiological functions. The tissue defects in this area not only seriously affect the physiological function, but also lead to facial deformity and aesthetic damage, affecting the quality of life of patients. The anterolateral thigh flap has become one of the main methods for defect repair due to its large tissue volume and high survival rate, and one of the key steps to ensure a high survival rate is the location of the perforator. How to find the perforator more accurately by improving the detection scheme or locating the perforator according to the anatomical structure, and guide the preparation and cutting of the flap, is the main direction of current research. This study intends to conduct a prospective diagnostic phase II clinical study on perforator localization of flap perforator, and explore its effectiveness and accuracy through sensitivity and specificity.

In this study, a total of 76 patients with maxillofacial defects caused by tumors, trauma and other reasons requiring anterolateral femoral flap repair were included, and the perforator branch of femoral anterolateral flap was positioned preoperatively by means of perforator positioning device and color Doppler ultrasound. After the anterolateral thigh flap was prepared, the incision was closed in the donor area of the leg, and the flap was transplanted free to the maxillofacial defect area for repair. The sensitivity, specificity, positive predictive value, negative predictive value, distance difference and odds ratio of the two methods were calculated respectively, and the differences of each evaluation index between the two groups were compared, mainly to evaluate the sensitivity and specificity between the two groups.

Enrollment

82 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. All patients with oral and maxillofacial defects caused by malignant tumors or trauma require anterior lateral femoral skin flap repair after surgery
  2. There is no history of leg trauma and surgery is feasible
  3. No clinically significant positive signs were found in physical examination
  4. No chronic or current illnesses such as heart, liver, pancreas, spleen, kidney, digestive tract, respiratory, blood, nervous system, etc
  5. No abnormalities found in electrocardiogram (ECG) and X-ray film
  6. Hepatitis B surface antigen (HBSAg), anti hepatitis C antibody (anti HCV), anti human immunodeficiency virus antibody (anti HIV), and negative Treponema pallidum (TP)
  7. No clinically significant abnormalities were found in vital signs, blood routine, urine routine, blood biochemistry, and blood pregnancy tests
  8. The patient voluntarily participated in this study and signed an informed consent form

Exclusion Criteria

  1. Have a history of leg injury or surgery
  2. Significant abnormalities in blood routine, heart, lung, liver, and kidney functions, insufficient compensatory function, or severe systemic diseases
  3. Pregnant or lactating women, or those planning to conceive within six months
  4. Individuals with a history of mental illness who cannot cooperate with the examination
  5. Individuals with allergic constitution or known allergies to contrast agent ingredients
  6. The patient or guardian refuses to sign a written consent form

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

82 participants in 1 patient group

perforator localization
Experimental group
Description:
CT and color Doppler ultrasound were used to locate the perforating branch of the descending branch of the lateral circumflex femoral artery, and the position of the perforator was compared with real perforator respectively during the operation.
Treatment:
Device: perforator locator

Trial contacts and locations

1

Loading...

Central trial contact

Qunxing Li; Bin Wei

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems