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Not yet recruiting NCT07353411

To Evaluate the Effectiveness and Safety of Single-port Robotic-assisted Subcutaneous Gland Resection in Males

No phase Interventional Gynecomastia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Single-port Robotic-assisted Subcutaneous Gland Resection in males.
Who it may be relevant to
Registry conditions: Gynecomastia. Basic parameters: 17 years — 75 years · Male.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Prospective, Single-center, Single-arm Clinical Study to Evaluate the Effectiveness and Safety of Single-port Robotic-assisted Subcutaneous Gland Resection in Males

Overview

The new technology of robotic surgery system, as an emerging technology, has shown certain application prospects in breast surgery. However, the new technology of robotic surgery system in China in the treatment of gynecomastia is still in the exploratory stage and needs to be further improved. This prospective, single-center, single-arm clinical study was conducted to use the single-port robot and evaluate the effectiveness and safety of the subcutaneous gland resection in the treatment of gynecomastia.

Detailed description

The new technology of robotic surgery system, as an emerging technology, has shown certain application prospects in breast surgery. However, the new technology of robotic surgery system in China in the treatment of gynecomastia is still in the exploratory stage and needs to be further improved. This prospective, single-center, single-arm clinical study was conducted to use the single-port robot and evaluate the effectiveness and safety of the subcutaneous gland resection in the treatment of gynecomastia.

Interventions

  • Procedure Single-port Robotic-assisted Subcutaneous Gland Resection in males
    Single-port Robotic-assisted Subcutaneous Gland Resection for males in the treatment of gynecomastia.

Primary outcome measures

  • Patient's and doctor's satisfaction [Time frame: 2 years]
  • Patient's psychological status using the Self Rating Anxiety Scale (SAS) [Time frame: 2 years]
  • Patient's psychological status [Time frame: 2 years]
  • Patient's sensory [Time frame: 2 years]

Eligibility criteria

Inclusion criteria

  • Male patients, aged 18-75 years old;
  • Preoperative breast ultrasound indicates male breast development, and breast enlargement symptoms persist for more than 1 year;
  • Primary male breast development that has been unresponsive to drug treatment, or those who refuse drug treatment;
  • According to Gynecomastia's surgical indications, refer to the "2023 Expert consensus on the clinicaldiagnosis and treatment of gynecomastia in China" Simon grading of male breast development IIb or above;
  • Due to social pressure or severe psychological burden caused by symptoms such as breast pain, those who have a strong desire for surgery may experience psychological burden caused by the disease and actively request surgery;
  • Individuals without serious accompanying diseases;
  • Suspected malignant transformation;
  • No other serious underlying diseases in the past;
  • The surgical procedure includes a single hole robot (intraperitoneal endoscopic single hole surgical system SP1000) for subcutaneous gland resection of the breast;
  • Participants are able to understand the research process, voluntarily join the study, sign informed consent forms, have good compliance, and cooperate with follow-up;
  • No swallowing difficulties; No shoulder joint movement disorders;
  • Complete clinical data.

Exclusion criteria

  • Age<16 years old, still in puberty, or disease duration ≤ 1 year;
  • Simple obesity, no obvious glandular tissue was found on breast ultrasound examination;
  • Male patients with breast developmental disorders secondary to other diseases;
  • Patients with contraindications for general anesthesia surgery such as coagulation dysfunction and severe cardiovascular disease, who cannot tolerate surgery;
  • The clinical data is basically incomplete;
  • Other surgical methods;
  • Individuals with a history of breast surgery or breast tumors in the past;
  • The serious diseases of non malignant tumors such as congenital testicular hypoplasia syndrome, cirrhosis, primary hypogonadism, and hyperthyroidism will affect the patient's compliance or put the patient in a dangerous state;
  • Dementia, intellectual disability, or any mental illness that hinders understanding of informed consent forms;
  • Lack of trust in surgical outcomes and weak desire for surgery.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07353411 · DQ-GYN-Robot-20251010

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗