Skip to content

Pilot study on intersegmental line identification during lung segmentectomy by video pulse wave extraction technology using non-contact vital sensing software

Pilot study on intersegmental line identification during lung segmentectomy by video pulse wave extraction technology using non-contact vital sensing software

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042240027
Enrollment
5
Registered
2024-05-16
Start date
2024-05-16
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

Metastatic lung tumor, Primary lung cancer

Interventions

During pulmonary segmentectomy, intraoperative videos are captured and analyzed using the non-contact vital sensing software. Subsequently, adverse events occurring within 30 days postoperatively are

Sponsors

Ohde Yasuhisa
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) age >=18 2) ECOG performance status (PS) is 0, 1, or 2. 3) Planning a pulmonary segmentectomy. 4) Planning to use the indocyanine green (ICG) method for intersegmental line identification. 5) Major organ function other than the lungs is preserved, and the physician determines that general anesthesia is feasible. 6) The patient has given a full explanation of the study and obtained written consent prior to enrollment in the study.

Exclusion criteria

Exclusion criteria: (1) A patient with a history of iodine sensitivity. (2) A patient with a history of hypersensitivity to components of ICG. (3) Pregnant women, breastfeeding women, and women who may be pregnant (4) Patients with a history of serious hypersensitivity (5) Patients deemed inappropriate for registration by the physician in charge.

Design outcomes

Primary

MeasureTime frame
The pulse wave identification rate of the non-contact vital sensing software in areas not planned for resection.

Secondary

MeasureTime frame
Non-identification rate of pulse waves by the non-contact vital sensing software in the planned resection area. Pulse wave identification rate of the non-contact vital sensing software on the lung surface before pulmonary artery and vein dissection. Adverse events within 30 days postoperatively.

Contacts

Public ContactShinya Katsumata

Shizuoka Cancer Center

shi.katsumata@scchr.jp+81-55-989-5222

Outcome results

None listed

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