Single-Port SHURUI Robotic Thoracic Surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the SHURUI single-port surgical robot (SR-ENS-600) used in thoracic and related surgeries. Eligible adults aged 18-75 with resectable lung cancers, oligometastatic lung disease, or mediastinal tumors may undergo endoscopic procedures with the robotic system. The investigation focuses on surgical feasibility, safety, and perioperative outcomes in a real-world clinical setting. Procedures involve limited-incision, single-port access to improve precision and potentially shorten recovery. Data collection includes standard perioperative metrics and patient outcomes, without a specified intervention arm since this is observational.

Why it matters

Who can join: the full rules

Inclusion criteria:

1. Age between 18 - 75 years;
2. Subjects need to undergo endoscopic surgery and meet one of the following indications for surgical treatment:

   * Lobectomy, segmentectomy wedge resection of lung: Clinically diagnosed resectable early stage non-small cell lung carcinoma; oligometastatic cancer to the lung;
   * Mediastinal mass resection: Clinically diagnosed mediastinal tumour (benign or malignant) that are indicated for resection;
3. Preoperative ASA grade: Grade I-III;
4. Subject voluntarily participates in the clinical trial, and agrees or his/her guardian agrees and signs the informed consent.

Exclusion criteria:

1. Subjects with a previous history of thoracic surgery or other malignant tumor which, in the judgement of the investigator, make them unsuitable for enrolment;
2. Subjects with severe co-morbidities or organ dysfunction (heart, lung, liver, brain, kidney, etc.) or deemed too weak/ unsuitable for general anesthesia or operation;
3. Non-correctable coagulopathy and severe bleeding tendency；
4. Emergency surgery;
5. Severe obesity with BMI ≥30 kg/m2;
6. Subjects with severe allergic constitution, suspected or confirmed alcohol, drug addiction;
7. Other circumstances in which the investigator considered participation in this clinical trial inappropriate.

Where it's running

• Prince of Wales Hospital
  Shatin, Hong Kong Recruiting

Study contacts

• Study coordinator: Calvin Sze Hang Ng
• Email: calvinng@surgery.cuhk.edu.hk
• Phone: +852 3505 2618

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.