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Randomized control study comparing quality of life after single-port versus conventional 3-port video-assisted thoracoscopic surgery

Randomized control study comparing quality of life after single-port versus conventional 3-port video-assisted thoracoscopic surgery - Randomized control study comparing single-port versus 3-port video-assisted thoracoscopic surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015340
Enrollment
84
Registered
2014-10-03
Start date
2014-10-03
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

primary lung cancer, metastatic lung cancer, benign tumor of the lung, pneumothorax

Interventions

single-port video-assisted thoracoscopic surgery partial resection Conventional 3-port video-assisted thoracoscopic surgery partial resection

Sponsors

Center of Chest Medicine and Surgery, Ehime University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients who need to undergo thoracoscopic lung partial resection for primary lung cancer, metastatic lung cancer, benign lung tumor, inflammatory lung nodule, or spontaneous pneumothorax (2)Patients who are tolerable for general anesthesia (3)Patients who are over 20 years of age at the time of consent (4)Patients who have not gotten ipsilateral thoracic surgery (5)Patients who received informed consent to attend this study, and the agreements are provided in a document

Exclusion criteria

Exclusion criteria: (1) Severe pulmonary diseases (2) Respiratory tract infection (3) Severe circulatory diseases (4) When performing another operation concurrently (5) Obesity (BMI:Body Mass Index over 35) (6) Suspected cases of pregnancy (7) Patients with mental disorder or dementia (8) Patients who are judged ineligible by the investigator and the attending surgeon

Design outcomes

Primary

MeasureTime frame
degree of postoperative pain (POD 1, Numeric Rating Scale (NRS))

Secondary

MeasureTime frame
intraoperative blood loss, duration of the surgical procedure, frequency of intraoperative and postoperative complications, distance from nodules or bullae to be resected to the edges, degree of postoperative pain (POD 2 to 5, Numeric Rating Scale (NRS)), frequency in use of analgesics, patient satisfaction score, postoperative pulmonary function, 6-munutes walk, CRP, WBC count, duration of drainage, postoperative hospital stay

Countries

Japan

Contacts

Public ContactYS Yoshifumi

Ehime University Hospital Center of Chest Medicine and Surgery

ysano@m.ehime-u.ac.jp+81899605331

Outcome results

None listed

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