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EQUIP study

Evaluation of postoperative pain by Pain Vision PS-2100, a quantitative an alyzer for perception and pain in pulmonary resection

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1042220032
Enrollment
50
Registered
2022-06-12
Start date
2022-07-25
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 tumors

Interventions

Measurement of pain degree by Pain Vision and N RS in Postoperative Pain

Sponsors

Ode Yasuhisa
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients 20 years of age or older who are schedule d for lobectomy or segmentectomy for lung tumors

Exclusion criteria

Exclusion criteria: (1) Patients who are scheduled to undergo chest wall resection (2) Patients with a history of open chest surgery (including thoracoscopic surgery) (3) Patients who are expected to have severe intrathoracic adhesions (4) Patients with heart failure or severe hepatic or renal dysfunction (5) Patients with psychiatric, cognitive, or neurological disorders, or a history of such disorders (6) Patients who are taking regular analgesics or c entral nervous system agents (7) Patients treated for skin diseases (8) Patients with cardiac pacemakers or other elec tronic implants

Design outcomes

Primary

MeasureTime frame
Association between NRS and pain degree using correlation coefficient on the first day after surgery

Secondary

MeasureTime frame
Association between NRS and pain degree using correlation coefficient on days 2, 5 and 7 after surgery Comparison of NRS and pain degree in patient background factors (gender, age, surgical technique,analgesics, etc.)

Contacts

Public ContactTatsuya Masuda

Shizuoka Cancer Center

ta.masuda@scchr.jp+81-55-989-5222

Outcome results

None listed

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