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Study on the Efficacy of Laparoscopic-Assisted Thyroglossal Duct Cyst Resection Via Submental Approach

19 de agosto de 2026 actualizado por: Guangjun Tang, People's Hospital of Anshun City of Guizhou Province

Thyroglossal duct cysts are congenital diseases of the neck. Once detected, surgical treatment is the first choice. The traditional Sistrunk surgery has definite efficacy but leaves scars on the neck. With the popularization of the concept of minimally invasive surgery, the non-inflated submandibular approach endoscopic technique provides a new idea for achieving a scar-free resection of the neck. This project intends to conduct a randomized controlled study to scientifically evaluate the clinical efficacy and safety of submandibular approach endoscopic-assisted resection of thyroglossal duct cysts.

The study plans to include 60 newly diagnosed patients, randomly divided into the experimental group (submandibular approach endoscopic resection of thyroglossal duct cysts) and the control group (traditional open surgery). Systematically compare the perioperative indicators (operation time, intraoperative blood loss, average hospital stay), postoperative pain (VAS score), complications (infection, recurrence, injury of the sublingual nerve), and incision satisfaction (Vancouver Scar Scale) between the two groups.

This project is expected to establish a standardized surgical procedure, verify the superiority of this technique in achieving a scar-free neck while ensuring complete resection of the lesion, provide evidence-based medical evidence for the promotion of scar-free surgery in the neck, and have both clinical innovation and social benefits.

Descripción general del estudio

Estado

Aún no reclutando

Condiciones

Descripción detallada

1. Project-defined project goals and task requirements analysis 1.1 Project Goals 1.1.1 Overall Goal This project aims to conduct a prospective randomized controlled study to scientifically evaluate the clinical efficacy and safety of endoscopic-assisted thyroglossal duct cyst resection through an un-inflated submental approach, establish a standardized surgical procedure, and provide evidence-based medical evidence for the promotion of minimally invasive surgery with no neck scars.

1.1.2 Specific Goals 1.1.2.1 Efficacy Verification Goal Compare the differences in surgical time, intraoperative blood loss, hospital stay, and postoperative pain between the submental approach endoscopic surgery and the traditional Sistrunk surgery.

1.1.2.2 Safety Assessment Goal Monitor the incidence of complications and the 1-year recurrence rate of the two groups, ensuring that the recurrence rate of the observation group is controlled within 5% .

1.1.2.3 Aesthetic Effect Evaluation Goal Use the Vancouver Scar Scale (VSS) to evaluate the aesthetic appearance of the incision at 1, 3, and 6 months after surgery.

1.1.2.4 Technical Standardization Goal Summarize the key technical points and form a standardized surgical operation procedure.

1.2. Task Requirements Analysis 1.2.1 Clinical Requirements Thyroglossal duct cysts account for 75% of the spectrum of congenital diseases in the neck. Although the traditional Sistrunk surgery reduces the recurrence rate to below 5%, it leaves scars on the neck, causing psychological burden to patients. Therefore, a treatment plan that balances cure and aesthetics urgently needs to be established.

1.2.2 Technical Requirements The existing endoscopic approaches through the mouth, chest, and breast have high infection risks, large trauma range, and require inflation. The un-inflated submental approach utilizes the natural skin creases under the chin, has a short path, can directly handle the hyoid bone, and combines aesthetics with safety. However, it lacks large-sample randomized controlled studies for verification.

1.2.3 Evidence-Based Requirements Most existing studies are small-sample case reports and lack high-quality controlled studies [2]. Conducting rigorous randomized controlled trials to systematically compare the efficacy, safety, and aesthetic effects of the two surgical methods is an urgent need to promote clinical application.

1.2.4 Social Benefit Requirements Neck scars affect patients' self-confidence and quality of life. Achieving no-neck scars is an embodiment of the medical model's shift towards "physical and mental rehabilitation", with good social benefits and promotion prospects.

2 Project Objectives and Main Technical Difficulties and Issues in Task Resolution 2.1 Technical Difficulties in Laryngeal Bone Handling under Endoscopy 2.1.1 Description of the Difficulties The recurrence rate can be as high as 50% if the laryngeal bone is not handled thoroughly. Under the endoscopic view, the laryngeal bone is located deep within and has a hard texture. The primary difficulty is to precisely disarticulate it while avoiding damage to the hypoglossal nerve and the superior laryngeal nerve.

2.1.2 Solution Ideas Preoperative CT three-dimensional reconstruction is used to predict the resection range; during the operation, an ultrasonic bone knife is used for precise disarticulation; the "five-step method" is adopted as the standard operating procedure; intraoperative nerve monitoring is used to assist in protecting the nerves.

2.2 Narrow Operating Space and Difficulties in Field Exposure 2.2.1 Description of the Difficulties There are no natural cavities in the neck, and the small incision under the chin placed with the endoscope leads to the "chopstick effect". The cyst is located below the laryngeal bone, and the field exposure is difficult.

2.2.2 Solution Ideas The non-inflated suspension method is used to establish the operating space; specialized and elongated endoscopic instruments are modified; the suspension tension is dynamically adjusted; the indications are strictly selected, excluding cases with a diameter > 4 cm or those in the infectious stage.

2.3 Identification and Protection of Important Nerves and Blood Vessels 2.3.1 Description of the Difficulties The submandibular area involves the hypoglossal nerve, superior laryngeal nerve, etc. The identification is difficult under the two-dimensional endoscopic view, and incorrect injury can lead to serious complications.

2.3.2 Solution Ideas The nerve is located by using the digastric muscle and masseter muscle as references ; the surgical field is kept blood-free; postoperative close observation of swallowing and speech functions is conducted.

2.4 Learning Curve and Standardization of Surgical Procedure 2.4.1 Description of the Difficulties The surgeon needs to have both open surgery experience and endoscopic skills. The initial operation time is longer (median 135 minutes), and there is a possibility of conversion to open surgery.

2.4.2 Solution Ideas Conduct anatomical training and simulation operations; formulate standardized surgical procedures; initially operated by experienced physicians; regularly analyze and summarize to continuously optimize.

2.5 Objective Evaluation of Aesthetic Effect 2.5.1 Description of the Difficulties Scar evaluation is subjective. How to objectively quantify the aesthetic effect is a research design difficulty.

2.5.2 Solution Ideas The Vancouver Scar Scale (VSS) is used to score from four dimensions: color, thickness, vascular distribution, and softness; combined with patient satisfaction VAS evaluation; third-party blind assessment is conducted.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

60

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Guang J Tang, MD
  • Número de teléfono: 86+ 13595302195
  • Correo electrónico: tgjdoctor@163.com

Copia de seguridad de contactos de estudio

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Niño
  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • The cyst is in the non-acute infection stage;

    • The cyst has not ruptured to form a skin sinus tract or fistula;

      • Preoperative B-ultrasound and CT indicated that it was a thyroglossal duct cyst;

        • There are no severe underlying heart or lung diseases or coagulation dysfunction;

          • The patient and their family voluntarily chose to undergo laparoscopic resection of the thyroglossal duct cyst; ⑥ The patient and their family voluntarily signed the informed consent form.

Exclusion Criteria:

  • The cyst is in the acute infection stage;

    • The cyst ruptures, forming a skin sinus tract or fistula; ③ Has severe underlying heart and lung diseases and coagulation dysfunction; ④ Those with cyst diameters greater than 4 cm; ⑤ Those currently participating in other research studies.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Submental endoscopic-assisted Sistrunk operation
After general anesthesia, the patient lies in a supine position with the neck slightly extended backward. A concealed incision of approximately 2-3 centimeters in length is made along the natural skin fold at about 1 centimeter below the chin (the submental area). Through this incision, a blunt dissection is performed at the subcutaneous thin muscle layer level to form a subcutaneous tunnel that extends directly to the thyroid cartilage region. The surgery is assisted by an endoscope with a suspension and traction system and without the need for inflation. Under high-definition endoscopic visualization, the thyroglossal duct cyst, the middle segment of the hyoid bone, and the path of the thyroglossal duct are carefully separated and completely resected. A closed drainage tube is placed. The submental incision is sutured using absorbable sutures within the dermis.
Make an incision in the middle of the skin on the neck, cut through the skin and subcutaneous tissue, expose the tumor and the hyoid bone, and completely remove the thyroglossal
Comparador activo: Conventional open Sistrunk operation via cervical incision
After general anesthesia, the patient is placed in the supine position with the neck extended. A horizontal skin incision is made along the midline of the neck directly over the thyroglossal duct cyst. The skin and subcutaneous tissues are divided. The strap muscles (sternohyoid and thyrohyoid) are separated in the midline to expose the cyst and the body of the hyoid bone. The thyroglossal duct cyst is dissected en bloc together with the central portion of the hyoid bone, preserving the surrounding vital structures. The surgical wound is thoroughly irrigated with normal saline. The incision is closed in layers with absorbable sutures, and a sterile dressing is applied.
After general anesthesia, the patient is placed in the supine position with the neck slightly extended. A concealed transverse skin incision of approximately 2-3 cm is made about 1 cm below the chin (submental area), following the natural skin creases. Through this incision, blunt dissection is performed in the subplatysmal plane to create a subcutaneous tunnel reaching the hyoid bone region. The operation is assisted by an endoscope with a suspended retractor system without gas insufflation, thus avoiding the risk of gas embolism. Under high-definition endoscopic visualization, the thyroglossal duct cyst, the middle segment of the hyoid bone, and the track of the thyroglossal duct are meticulously dissected and completely resected en bloc. Hemostasis is achieved carefully to preserve the recurrent laryngeal and hypoglossal nerves. The wound is thoroughly irrigated with normal saline. A closed suction drain is placed if necessary. The submental incision is closed with intradermal absor
Otros nombres:
  • Submental endoscopic-assisted Sistrunk operation

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Perioperative Clinical Indicators
Periodo de tiempo: Perioperative
Includes operation time (minutes), intraoperative blood loss (mL), and postoperative length of hospital stay (days).
Perioperative
Vancouver Scar Scale (VSS) Score
Periodo de tiempo: up to 6 mouth
VSS evaluates scars across 4 subscales: pigmentation, thickness, vascularity, and pliability. Subscale scores are summed to generate a total score (range 0-15, with higher scores reflecting more severe scarring).
up to 6 mouth
Pain Intensity assessed by Visual Analogue Scale (VAS)
Periodo de tiempo: up to 72 hours
A 10-cm horizontal line anchored by 0 (no pain) and 10 (worst imaginable pain). Participants mark a point corresponding to their current pain level. Higher scores indicate worse pain.
up to 72 hours

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Total Postoperative Negative-Pressure Wound Drainage Volume
Periodo de tiempo: up to Day 2
Total volume (mL) of fluid collected from the surgical site via closed suction drainage prior to drain removal.
up to Day 2

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Director de estudio: fei L Yue, PG, People's Hospital of Anshun City of Guizhou Province

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

30 de junio de 2028

Finalización del estudio (Estimado)

30 de junio de 2028

Fechas de registro del estudio

Enviado por primera vez

8 de julio de 2026

Primero enviado que cumplió con los criterios de control de calidad

19 de agosto de 2026

Publicado por primera vez (Actual)

21 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

21 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

19 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • PHAnshun2
  • An City Office [2026] No. 6 (Otro número de subvención/financiamiento: Anshun Municipal Bureau of Science and Technology)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

Sí

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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