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Comparison study of subclavian approach endoscopic thyroid surgery and non-inflatable transaxillary approach endoscopic thyroid surgery

Comparison study of subclavian approach endoscopic thyroid surgery and non-inflatable transaxillary approach endoscopic thyroid surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086466
Enrollment
Unknown
Registered
2024-07-02
Start date
2023-12-15
Completion date
Unknown
Last updated
2024-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

thyroid diseases

Interventions

observation group:subclavian approach endoscopic thyroid surgery
control group:non-inflatable transaxillary approach endoscopic thyroid surgery

Sponsors

The Affiliated Lihuili Hospital of Ningbo University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 99 Years

Inclusion criteria

Inclusion criteria: ?Benign thyroid nodules, adenomas and other thyroid nodules requiring surgery, with a maximum diameter of <6cm (cystic can be relaxed to 6-8cm); ?Differentiated thyroid cancer simultaneously meets the following conditions: a. the maximum diameter of the primary lesion is <2cm, b. there is no extrathyroidal invasion or only a small extrathyroidal invasion lesion that breaks through the anterior thyroid capsule or a small invasion of the sternocleidomastoid muscle, cN0; ?The patients have high cosmetic requirements and require endoscopic surgery; ?The patients and their families informed consent and signed the informed consent form for this study.

Exclusion criteria

Exclusion criteria: ?Previous history of neck, subclavian and axillary surgery, radiotherapy or thermal ablation; ?With heart, liver, kidney and other organ dysfunction that cannot tolerate surgery; ?Combined with other malignant tumors; ?Differentiated thyroid cancer with poor prognosis pathological subtypes, dedifferentiated thyroid cancer; ?Combined with hyperthyroidism; ?Thoracic deformity; ?Incomplete case data.

Design outcomes

Primary

MeasureTime frame
operation time;intraoperative bleeding;postoperative drainage;the placement time of drainage tube;hospitalization time;the complete exposure rate of the central compartment;the number of positive central compartment lymph nodes/ the number of central compartment lymph nodes;postoperative complication;postoperative swallowing function score;operating area pain score;operating area numbness score;incision scar satisfaction score;surgical incision concealment score;incision pain satisfaction score;

Countries

China

Contacts

Public ContactGaoxiang Chen

The Affiliated Lihuili Hospital of Ningbo University, Ningbo, Zhejiang, 315040, P. R. China

xtkxcgx@126.com+86 153 8139 7967

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026