Risk factor analysis for nausea and vomite induceded by narcotic drugs, multi center trial.

Risk factor analysis for nausea and vomite induceded by narcotic drugs, multi center trial. - Risk factor analysis for nausea and vomite induceded by narcotic drugs, multi center trial.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000008450

Enrollment

400

Registered

2012-07-17

Start date

2012-05-01

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

cancer pain

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: All malignant disease patients who have no further history of Narcotic drugs administration. Histopathology stage : no restriction Agreement document : required

Exclusion criteria

Exclusion criteria: Narcotic drugs only single administration. (Not routine use.) Withdrawal administration except a reason of nausea/vomit. History of Codeine phosphate , Tramadol Hydrochloride, Pentazocine, Buprenorphine administration.

Design outcomes

Primary

Measure	Time frame
We analyze correlation between Patient background factor and nausea/vomit incidence for 7days after narcotic drugs administration.	—

Countries

Japan

Contacts

Public ContactHiroshi Ueda

Itami City Hospital Pharmacy

ueda-itm@umin.ac.jp0727773773

Outcome results