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


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Pain

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Trial Information

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


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.


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

Type of Study:

Observational

Study Design:

Observational Model: Case-Only, Time Perspective: Prospective

Outcome Measure:

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

Outcome Time Frame:

6 Years

Safety Issue:

No

Principal Investigator

Prachee Singh, BS

Investigator Role:

Principal Investigator

Investigator Affiliation:

M.D. Anderson Cancer Center

Authority:

United States: Institutional Review Board

Study ID:

ID02-374

NCT ID:

NCT00500942

Start Date:

January 2003

Completion Date:

June 2009

Related Keywords:

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

Name

Location

U.T.M.D. Anderson Cancer Center Houston, Texas  77030