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Evaluation of perioperative respiratory management after lung resection using displacement sensor

Evaluation of perioperative respiratory management after lung resection using displacement sensor - Respiratory management after lung resection with displacement sensor

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031533
Enrollment
60
Registered
2018-03-01
Start date
2018-03-15
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

lung cancer

Interventions

method Measurement method: Install a displacement sensor with a pad similar to the electrocardiogram so as to cross obliquely across the 6th and 9th intercostal spaces on both sides. For the operativ

Sponsors

Tokyo Medical and Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.A non-small cell lung cancer patient who is scheduled to perform a pulmonary resection operation 2.Those who are not diagnosed with pulmonary emphysema/interstitial pneumonia due to preoperative examination and do not show decreased respiratory function. 3.The presence of interstitial pneumonia is confirmed on the image. Information that can be observed for more than 30 days after surgery, information such as patient background, perioperative factor, prognosis, presence or absence of acute exacerbation can be obtained or expected to be possible. Those that are expected to be able to acquire these information even in the case of death within 30 days. 4.For preclinical pulmonary function tests, those classified as 2 degree or more (%FEV1 <70%) by Gold classification are targeted. It does not matter whether or not internal or inhalation therapy for pulmonary emphysema is present. It is possible to observe 30 days or more postoperatively, and information such as patient background, perioperative factor, prognosis etc. can be acquired or expected to be possible. Those that are expected to be able to acquire these information even in the case of death within 30 days. 5.Agreement When aged 20 years or older 6.Patients who gave sufficient consultation on participation of this study and obtained consent

Exclusion criteria

Exclusion criteria: 1)There is a history of allergy to the material 2)not attach sensor due to complications of skin diseases 3)difficult to self-decide due to dementia, disorientation of consciousness, etc. 4) Other cases that the investigator considered to be inappropriate as the subject of this study

Design outcomes

Primary

MeasureTime frame
Relationship between measured respiratory measurements and postoperative respiratory complications within 7 days after surgery

Countries

Japan

Contacts

Public ContactKobayashi Masashi

Tokyo Medical and Dental University Thoracic Surgery

mkobthsr@tmd.ac.jp03-5803-0375

Outcome results

None listed

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