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The Effect of Cancer Pain Management Protocol on Hospitalized Cancer Patients: A Pilot Study

A Pilot Study: The Effect of Cancer Pain Management Protocol on Hospitalized Cancer Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01043068
Enrollment
25
Registered
2010-01-06
Start date
2010-01-31
Completion date
2010-12-31
Last updated
2012-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancers, Pain

Keywords

cancer pain, opioid, guideline

Brief summary

The purpose of this study was to prospectively evaluate the effect of cancer pain management protocol on hospitalized cancer patients.

Interventions

Interventions based on published pain guideline. The interventions consisted of the following: (1) nursing pain assessment of current pain, worst pain, pain relief, and acceptability of pain; (2) feedback to guide analgesic prescribing by physician.

Sponsors

Janssen Korea, Ltd., Korea
CollaboratorINDUSTRY
National Cancer Center, Korea
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hospitalized patient with the somatic and/or visceral pain having an untreated intensity greater than 3 on a 10 cm visual analog scale (VAS; 0 = no pain, 10 = unbearable pain)over the week prior to enrollment * A minimum age of 18 years

Exclusion criteria

* Opioid intolerance * No longer treatment for their underlying disease. * Intracerebral primary or metastatic lesion * Impaired sensory or cognitive function * Pregnant or lactating woman * Women of child bearing potential not using a contraceptive method * Sexually active fertile men not using effective birth control during medication of study drug and up to 6 months after completion of study drug if their partners are women of child-bearing potential * Any patients judged by the investigator to be unfit to participate in the study

Design outcomes

Primary

MeasureTime frame
Reduction in pain scoresJan 2010 - October 2010

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026