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Pain Quantification and Pain Management in Interventional Radiology (IR)

Pain Quantification and Management for Standard Interventional Radiology (IR) Procedures With Subsequent Patient Satisfaction Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00500942
Enrollment
374
Registered
2007-07-13
Start date
2003-01-31
Completion date
2009-06-30
Last updated
2012-08-02

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

Conditions

Pain

Keywords

Interventional Radiology, Pain Quantification, Pain Management, Patient Satisfaction, Questionnaire, Survey

Brief summary

Primary Objectives: * To measure and record patients' pain levels before, during, and after standard procedures performed in IR. * To compare different procedures to respective pain levels and patient satisfaction (as determined by questionnaire).

Detailed description

During the IR procedure, nurses commonly ask patients to tell them what their pain level is on a 0-10 scale. For those who participate in the study, these numbers will be used to calculate average pain levels. Study participants will be asked to complete the same 0-10 pain scale during the recovery period until time of discharge or admission to the hospital. According to standard criteria when giving conscious sedation, patients will remain in a communicable state throughout the procedure and during the recovery period prior to discharge, and thus, will be able to express a pain level during these times. The same questionnaire will be given for seven days after the procedure, which will be completed on a self-addressed, stamped postcard to be mailed back to UTMDACC. The last postcard will have a couple of questions about patient satisfaction. Once the last postcard is mailed in, the patient's participation in the study is over. Each questionnaire should take less than 5 minutes to complete. This is an investigational study. About 374 patients will take part in this study. All will be enrolled at UTMDACC.

Interventions

BEHAVIORALQuestionnaire

Questionnaires about the pain level experienced during and after standard procedures are performed in the IR.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Scheduled for an IR procedure at UTMDACC * Lives in the United States (easier to contact patients via phone/mailings) * English-speaking * Provide written informed consent

Exclusion criteria

* Refusal to participate * Current diagnosis of mental illness, such as psychosis or dementia * Procedure performed under monitored anesthesia care (MAC), general endotracheal anesthesia (GETA), or local anesthesia care

Design outcomes

Primary

MeasureTime frame
To measure and record patients' pain levels before, during, and after standard procedures performed in Interventional Radiology (IR).6 Years

Secondary

MeasureTime frame
To find a standard method of pain management for each procedure type.6 Years

Countries

United States

Outcome results

None listed

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