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Retrospective multicenter clinical study of Conversion rate of hydromorphone in cancer patients

Not Applicable
Recruiting
Conditions
cancer
Registration Number
JPRN-jRCT1040220043
Lead Sponsor
akamura Kazuyo
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Inpatients who changed the route of hydromorphone from injectable to oral

Exclusion Criteria

(1)Patients treated with chemotherapy or radiotherapy in the 24 hours before and after rerouting
(2)Patients who were using opioids other than hydromorphone
(3)Patients with difficulty in pain assessment

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The conversion ratio from intravenous hydromorphone to oral hydromorphone
Secondary Outcome Measures
NameTimeMethod
Factors affecting conversion ratios
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