Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
ID06468696

Improvements in Thyroid Tumor Surgery and the Prognosis, Diagnosis, Recurrence and Metastasis of Patients

Led by Second Affiliated Hospital of Xi'an Jiaotong University · Updated on 2024-06-21

170

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating improved surgical techniques for transthoracic endoscopic thyroidectomy, focusing on whether omitting the cervical linea alba suture can reduce operation time, postoperative pain, and incision complications. The study also aims to collect normal thyroid tissues, benign and malignant tumors, and lymph nodes to better understand the processes involved in the development, spread, and return of thyroid cancer. Participants will undergo either suturing or not suturing the cervical linea alba during minimally invasive thyroid surgery through a breast approach. The study involves collecting tissue samples including thyroid papillary carcinoma, adjacent thyroid tissue, and lymph nodes with or without metastasis. Transcriptome sequencing will be performed on collected tissues to analyze mRNA expression profiles within one month after surgery. During the study, participants will have preoperative assessments including ultrasound, CT scans, thyroid function tests, and fine-needle biopsies. Researchers will monitor outcomes such as postoperative neck swelling and pain within one week after surgery and analyze tissue gene expression. Participation involves routine clinical diagnosis, treatment, and tissue collection during surgery. The study is expected to last until January 2026 and involves about 200 volunteers.

CONDITIONS

Brief Title

Improvements in Thyroid Tumor Surgery and the Prognosis, Diagnosis, Recurrence and Metastasis of Patients

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Undergoing transthoracic endoscopic thyroidectomy via the breast approach
  • Postoperative pathology confirms benign or malignant thyroid tumors
  • Preoperative thyroid ultrasound or neck CT shows no tumor spread outside the thyroid or distant metastasis
  • No contraindications for general anesthesia
  • Patients with cosmetic concerns about surgical scars
Not Eligible

You will not qualify if you...

  • Previous transthoracic endoscopic thyroidectomy
  • Postoperative pathology confirms benign or malignant thyroid tumors (if already treated)
  • Preoperative thyroid ultrasound or neck CT shows tumor spread outside the thyroid or distant metastasis
  • Contraindications to general anesthesia
  • No cosmetic requirements for surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Surgery day and up to 1 week post-surgery

Participants undergo transthoracic endoscopic thyroidectomy via the breast approach with or without suturing the cervical linea alba, and receive immediate post-operative care.

Approximately 1 surgery visit and daily follow-up visits for up to 1 week

Post-operative Follow-up

Duration - Up to 1 month after surgery

Participants are monitored for short-term outcomes including neck edema and pain and tissue samples are collected for transcriptome sequencing analyses.

1 to 2 visits within one month post-surgery

Trial Site Locations

Total: 1 location

1

Xi'an Jiaotong University Second Affiliated Hospital

Xi'an, Shaanxi, China, 710049

Actively Recruiting

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Research Team

Z

Zhidong Wang, Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

6

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