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NCT Number: NCT07353411

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

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.

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Key information

Age range

17 year–75 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Single-port Robotic-assisted Subcutaneous Gland Resection in males

Procedure

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

Primary outcomes

  1. Patient's and doctor's satisfaction

    Time frame: 2 years

    Use the Health Status Survey Questionnaire (SF-36) to assess the general condition of patients.

  2. Patient's psychological status using the Self Rating Anxiety Scale (SAS)

    Time frame: 2 years

    Use the Self Rating Anxiety Scale (SAS) to assess the psychological status of patients.

  3. Patient's psychological status

    Time frame: 2 years

    Use the Self Rating Depression Scale (SDS) to assess the psychological status of patients.

  4. Patient's sensory

    Time frame: 2 years

    Using Semmes Weinstein (S-W) monofilament to detect postoperative sensory recovery in patients.

Study contacts

Contact information is provided by the study sponsor or research team.

Qiang Ding, Professor

CONTACT

[email protected]

13951731373

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital with Nanjing Medical University

Other

Registry information

Official study 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

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Jan 20, 2026
Registry last updated
Jan 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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