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A Multicenter Trial of PLA vs. Surgery for Treating PTMC

A Multicenter Prospective Controlled Trial of Laser Ablation Versus Surgery for the Treatment of Papillary Thyroid Microcarcinoma

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03377829
Enrollment
200
Registered
2017-12-19
Start date
2017-12-01
Completion date
2022-12-31
Last updated
2021-03-19

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

Conditions

Thyroid Cancer, Treatment Related Cancer

Keywords

Papillary Thyroid Microcarcinoma, Percutaneous Laser Ablation, thyroidectomy, ultrasonography, double-blind

Brief summary

This is a multicenter prospective controlled trial of percutaneous laser ablation(PLA) versus conventional surgery for the treatment of papillary thyroid microcarcinoma (PTMC).

Detailed description

PLA is the acronym for Percutaneous Laser Ablation. The treatment consists in the destruction (ablation) of Papillary Thyroid Micro Carcinoma by means of optical fibers that deliver high-energy light (laser) into the lesion through skin puncturing (percutaneous). The procedure is performed under ultrasound imaging guidance (ultrasound-guided). The destruction of the lesion occurs through overheating and coagulation. PLA, however, still needs a large-scale validation trial in order to be considered as an effective alternative to both surgery or follow-up for low-risk PTMC in elderly patients and/or in patients with co-morbidities that might expose the patients to a high surgical risk. After a comprehensive information, patients will be consecutively assigned to Group 1 (surgery, preferentially lobectomy) or to Group 2 (percutaneous laser ablation, performed according to the attached procedure).Peri and post-operative complications, need of drug treatment, length of hospital admission and customer satisfaction will be registered. The aims of this study are as follows: 1.To establish the rate of cure or partial ablation; 2.To compare the complication rate, time expenditure and costs of two procedures; 3.To assess changes in thyroid function and the need of substitution therapy with two procedures; 4.To assess the tolerability of the procedure, the customer satisfaction and the impact on the quality of life of the patients between conventional surgery and PLA.

Interventions

PROCEDUREPLA

During the PLA, the patient is in supine position with head extended: the physician, ultrasound assistant and trained nurse work within the sterile field. Under constant ultrasound image guidance and after local anesthesia by means of 2% xylocaine infiltration, thin needles (21G) are positioned in the thyroid lesion, within safety distance from the surrounding anatomical structures. A plane-cut tip fiber optics is inserted into the PTMC through the needle. The laser at 1064 nm wavelength is turned on for 10 minutes until the pre-established energy dose is attained. There is usually no pain or very limited pain.

PROCEDUREThyroid Surgery

Patients are routinely disinfected and spread the drapes after general anesthesia. Neck skin, fat, placenta muscle are incised successively. The flap is separated to the upper edge of thyroid cartilage, neck white line is incised and anterior muscle group is separated. Then both sides thyroid lobes are exposed. Cut off the isthmus, ligature the thyroid artery, cut off the upper pole. Ligature and cut off the ipsilateral thyroid vein. Reveal and protect the ipsilateral recurrent laryngeal nerve and the parathyroid gland during the entire process. Finally patient is performed total thyroidectomy or subtotal thyroidectomy.

Sponsors

WeiWei Zhan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed PTMC (maximun diameter\> = 5 mm and \< = 10 mm) proved by fine needle aspiration biopsy with good thyroid function; * Age≥ 18 Y; * Single nodule without thyroid capsule contact; * There had more than 3mm distance between nodules and trachea, carotid artery, recurrent laryngeal nerve (The distance should up to 5mm after injection of isolation fluid); * No coarse calcification or eggshell-like calcification; * Imaging examination without local or distant metastasis; * Without chemotherapy, radiotherapy and other related therapies; * A complete clinical, pathological and follow-up information; * Get informed consent signed by the patient or family member.

Exclusion criteria

* Multifocal PTMC; * Combined with other types of thyroid cancer or hyperthyroidism; * Lesion contact with thyroid capsule or located in the isthmus; * Serious coagulation dysfunction; * Contralateral vocal cord paralysis; * Imaging examination with local or distant metastasis; * Active Tuberculosis and HIV-positive patients; * Patients can not understand or follow research protocol; * Pregnant woman.

Design outcomes

Primary

MeasureTime frameDescription
Serological examination of thyroid functionup to 12 monthsHyperthyreosis or hypothyroidism.

Secondary

MeasureTime frameDescription
Recurrence rateup to 12 monthsThe recurrence rate in the thyroid bed or regional lymph-nodes
Therapeutic Effectup to 24 monthsThe rate of cure (defined as the absence of disease persistence at US examination and FNAB) between two methods.

Countries

China, Italy

Contacts

Primary ContactLu Zhang
aluer2013@163.com+8615021590551
Backup ContactWei Zhou
zw11468@126.com+8613681642667

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026