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Clinical Trials in China / NCT06398795
Recruiting Not applicable

Dual-port Trans-subclavian Thyroid Endoscopic Surgery

NCT06398795 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital of Wenzhou Medical University
Phase
Not applicable
Started
2022-09-01
Last updated
2024-12-31

Condition(s) studied

Thyroid NeoplasmsEndoscopic Surgery

Investigational drug(s) / intervention(s)

Dual-port Trans-subclavian Thyroid Endoscopic Surgery (DTS).Conventional open thyroidectomy (COT)

Dual-port Trans-subclavian Thyroid Endoscopic Surgery (DTS).: An innovative surgical approach, Dual-port Trans-subclavian Thyroid Endoscopic Surgery (DTS), presents a unique dual-port endoscopic technique for thyroidectomy. DTS significantly reduces postoperative hospital stay, emphasizing its potential for accelerated patient recovery compared to COT.

Conventional open thyroidectomy (COT): open thyroidectomy with traditional collar incisions

Study summary

This is a prospective, single-center, open-label, non-randomized controlled real-world study aimed at exploring a novel approach to cavity construction for thyroid endoscopic surgery. The study seeks to evaluate its effectiveness and safety while accumulating further evidence-based medical data.

Three hundred patients with thyroid tumors were divided into an experimental group (150 cases receiving a new endoscopic thyroid surgery technique, namely, dual-port trans-subclavian thyroid endoscopic surgery) and a control group (150 cases undergoing traditional open thyroid surgery) according to their treatment intention. Laboratory and medical data from specified follow-up points are collected, and adverse events are recorded detailly.

The primary efficacy endpoint is a comparison of surgical complications between the two treatment groups. Secondary endpoints include: (1) levels of IL-2, IL-4, IL-6, IL-10, TNF-α, INF-γ, renin, angiotensin II, and aldosterone preoperatively and on the second day postoperatively; (2) NRS scores on the first day postoperatively; (3) length of hospital stay, duration of surgery, total treatment cost, and postoperative drainage volume; and (4) assessment of wound satisfaction during a three-month follow-up visit.

Safety assessments include adverse events, vital signs, and pathological examinations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * Thyroid cancer or benign thyroid tumors * Patients with a demand for incisional cosmetic improvement Exclusion Criteria: * Patients with thyroid cancer larger than 2 cm * benign tumors larger than 5 cm * Patients with severe underlying diseases * Patients with chronic kidney disease, * Patients with autoimmune diseases * Patients with rheumatoid arthritis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
First Affiliated Hospital of Wenzhou Medical University Wenzhou Zhejiang Recruiting

More First Affiliated Hospital of Wenzhou Medical University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06398795 on ClinicalTrials.gov ↗ ← All trials in China