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Research on the effectiveness of wound protection in robot-assisted surgery

Research on the effectiveness of wound protection in robot-assisted surgery - Research on the effectiveness of wound protection in robot-assisted surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057585
Enrollment
30
Registered
2025-04-11
Start date
2025-04-26
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Robot-assisted lobectomy or equivalent surgery

Interventions

This is a study to evaluate whether the use of additional lap protectors MiniMIni, which are used in ordinary endoscopic surgery, enables surgeons to perform surgery smoothly and safely. In other word

Sponsors

Itabashi Chuo Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Preoperative 1. The patient is scheduled to undergo robot-assisted lobectomy or a similar procedure. 2. The patient is between 20 and 85 years old on the day of surgery. 3. ASA 1-2 4. Plt >=100,000, Cr<=2.0mg/dl 5. The patient has given written consent. During surgery The patient has undergone lobectomy (with lymph node dissection) or a similar procedure.

Exclusion criteria

Exclusion criteria: 1. Patients who have had a previous thoracotomy on the same side as the planned surgery due to a thoracic disease. 1. Patients with a history of tuberculosis or other conditions that may result in thoracic adhesions. 2. Patients with severe interstitial pneumonia, pulmonary fibrosis, or emphysema. 3. Patients with cirrhosis or renal failure. 4. Patients with a history of radiation therapy to the chest wall or thoracic cavity. 5. Patients with a history of allergy to local anesthetics or narcotics. 6. Pregnant or possibly pregnant. 7. Patients with psychosis or psychiatric symptoms that make it difficult to participate in the study. 8. Patients with active infection, serious cardiac complications, or poorly controlled diabetes.

Design outcomes

Primary

MeasureTime frame
Efficacy of reducing the number of lens cleaning procedures during surgery

Secondary

MeasureTime frame
Improvement in surgery time, improvement in wound crush, improvement in pain, stress reduction effect for staff involved during surgery

Countries

Japan

Contacts

Public ContactRei Kobayashi

Itabashi Chuo Medical Center Department of Thoracic Surgery

chinosenar@gmail.com03-3967-1181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026