Development and clinical application of single-port thoracoscopic minimally invasive surgical instruments

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037183

Enrollment

Unknown

Registered

2020-08-27

Start date

2021-10-01

Completion date

Unknown

Last updated

2020-10-05

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

Conditions

lung cancer

Interventions

New equipment group:surgery using new single-port endoscope instrument

normal equipment group:Surgery using traditional single port endoscopic instruments

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: a. 18-80 years old, no gender limit; b. Those who have no previous history of other cancers; c. Patients who meet the conditions of endoscopic surgery.

Exclusion criteria

Exclusion criteria: a. Intraoperative bleeding cannot be controlled and turned to thoracotomy; b. Intraoperative lymph node resection is difficult to switch to multi-hole endoscopy and thoracotomy.

Design outcomes

Primary

Measure	Time frame
survival time;operative time;blood loss in operation;	—

Countries

China

Contacts

Public ContactXiaogang Zhao

Shanghai Pulmonary Hospital

xiaobenben20000cn@163.com+86 18616587602

Outcome results

None listed

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