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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06468696
Other study ID # 20230318
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date January 1, 2026

Study information

Verified date June 2024
Source Second Affiliated Hospital of Xi'an Jiaotong University
Contact Zhidong Wang, Professor
Phone +86 138 9182 3580
Email xawzd@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this research is to investigate the clinical outcomes of modified surgical techniques such as omitting the cervical linea alba suture in transthoracic endoscopic thyroidectomy. Furthermore, the study requires the collection of normal thyroid tissues, benign and malignant thyroid tumors, and lymph nodes to further clarify the mechanisms associated with the initiation, progression, metastasis, and recurrence of thyroid cancer.


Description:

Study Purpose: Background and Significance Trans-axillary and trans-breast endoscopic thyroid surgery is currently the most widely used and recognized minimally invasive cosmetic thyroid surgery method. However, due to its inherent characteristics, this approach still has certain limitations that require further improvement. For example, there have been no studies reporting the short-term and long-term advantages of not suturing the cervical white line during trans-breast endoscopic thyroid surgery. Through theoretical analysis, it is suggested that not suturing the cervical white line during endoscopic thyroid surgery might be safe and feasible in terms of reducing operation time, postoperative pain, and incision complications, but this needs to be further verified. The mechanisms underlying the occurrence, progression, metastasis, and recurrence of thyroid cancer are still not completely understood, necessitating further basic and clinically relevant research using clinical specimens. Combining the current research progress domestically and internationally, the purpose of this study is to explore the clinical outcomes of improved surgical methods, such as not suturing the cervical white line during trans-axillary and trans-breast endoscopic thyroidectomy. In addition, the study aims to collect normal thyroid tissue, benign and malignant thyroid tumors, and lymph nodes to further elucidate the mechanisms related to the occurrence, progression, metastasis, and recurrence of thyroid cancer. Study Procedure Before you are enrolled in the study, the doctor will conduct a detailed inquiry and record your medical history. Preoperative evaluations will include thyroid and lymph node ultrasound, neck CT, thyroid function tests, and fine-needle aspiration biopsy. If you meet the inclusion and exclusion criteria, you can voluntarily choose to participate in this study and sign an informed consent form. If you agree to participate in this study, you will be assigned a number, and a research file will be created. This study will be conducted at the Second Affiliated Hospital of Xi'an Jiaotong University, with an estimated 200 voluntary participants. The research will involve collecting medical information data generated during routine clinical diagnosis and treatment, pathological reports, and tissue specimens from the thyroid, thyroid tumors, and lymph nodes obtained during surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 170
Est. completion date January 1, 2026
Est. primary completion date January 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Perform transthoracic endoscopic thyroidectomy via breast approach; 2. Postoperative pathology confirms benign or malignant thyroid tumors; 3. Preoperative thyroid ultrasound or cervical CT suggests no extrathyroidal invasion or distant metastasis of the tumor; 4. No contraindications for general anesthesia; 5. Patients with cosmetic requirements. Exclusion Criteria: 1. Underwent transthoracic endoscopic thyroidectomy; 2. Postoperative pathology confirmed as benign or malignant thyroid tumors; 3. Preoperative thyroid ultrasound or neck CT suggested no extraglandular invasion or distant metastasis of the tumor; 4. No contraindications to general anesthesia; 5. Patients with cosmetic demands.

Study Design


Intervention

Procedure:
Suturing the cervical linea alba during endoscopic thyroid surgery.
Suturing the cervical linea alba during endoscopic thyroid surgery.
Genetic:
Performing transcriptome sequencing
Performing transcriptome sequencing

Locations

Country Name City State
China Xi'an Jiaotong University Second Affiliated Hospital Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital of Xi'an Jiaotong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative neck edema Incidence rate Postoperative neck edema Incidence rate Within one week post-surgery
Primary Postoperative short-term pain Record the patient's perception of wound pain on postoperative days 1, 3, and 5 using the Numerical Rating Scale (NRS), which ranges from 0 (no pain) to 10 (worst pain), for quantification. Within one week post-surgery
Primary Thyroid Papillary carcinoma tissue mRNA expression profile After extracting total RNA from tissue, it is purified and a cDNA library is constructed. Following library quality control, sequencing is conducted on the Illumina NovaSeq 6000 platform using the PE150 mode to obtain tissue mRNA expression data. Within one month after the transcriptome sequencing.
Primary Thyroid papillary carcinoma metastatic lymph node mRNA expression profile After extracting total RNA from tissue, it is purified and a cDNA library is constructed. Following library quality control, sequencing is conducted on the Illumina NovaSeq 6000 platform using the PE150 mode to obtain tissue mRNA expression data. Within one month after the transcriptome sequencing.
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