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Multi-center Exploratory Controlled before-after Study for Efficacy and Safety of the Reducing Clinician Burden with Standardized Clinical Pathways

Multi-center Exploratory Controlled before-after Study for Efficacy and Safety of the Reducing Clinician Burden with Standardized Clinical Pathways - Multi-center Exploratory Controlled before-after Study for Efficacy and Safety of the Reducing Clinician Burden with Standardized Clinical Pathways

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000048403
Enrollment
4500
Registered
2022-07-20
Start date
2022-08-15
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

Arrhythmia, angina pectoris, acute myocardial infarction, lung cancer

Interventions

There are a total of 4,500 cases. There are 3,000 cases of three cardiovascular area pathways (1,000 cases at each facility) and 1,500 cases of VATS pathway for respiratory surgery (500 cases at each

Sponsors

Kyushu University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Those for which written consent has been obtained by the free will of the person himself / herself. Those who are 18 years of age or older at the time of patient registration. Occupation of a physician, nurse, or clinical laboratory technologist. Those who have been in business for more than 5 years at the time of registration. Those who are enrolled in the laboratory facility throughout the study period. (1) Adult cases in which the radiofrequency catheter ablation pathway or percutaneous coronary intervention pathway or acute myocardial infarction pathway is applied in the cardiovascular ward at Kyushu University Hospital, Saiseikai Kumamoto Disease, and NTT East Kanto Hospital. (2) Adult patients applying vats lobectomy for lung cancer pathway at Kyushu University Hospital, Saiseikai Kumamoto Hospital, and Shikoku Cancer Center in respiratory surgery wards.

Exclusion criteria

Exclusion criteria: Those who are judged by the investigator to be inappropriate for intervention in this study.

Design outcomes

Primary

MeasureTime frame
The amount of change in average total time of physicians from baseline after the pathway revision.

Secondary

MeasureTime frame
The amount of change in average total time of nurses and clinical laboratory technicians from baseline after the pathway revision.

Countries

Japan

Contacts

Public ContactTakanori Yamashita

Kyushu University Hospital Medical Information Center

yamashita.takanori.804@m.kyushu-u.ac.jp0926425881

Outcome results

None listed

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