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OpenTrials
Completed

NCT Number: NCT00500942

Pain Quantification and Pain Management in Interventional Radiology (IR)

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).

Completed

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Questionnaire

Behavioral

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

Other names: Survey

Primary outcomes

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

    Time frame: 6 Years

Secondary outcomes

  1. To find a standard method of pain management for each procedure type.

    Time frame: 6 Years

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Official study title

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

Important dates

Study start
2003
Primary completion
2009
Study completion
2009
First posted
Jul 13, 2007
Registry last updated
Aug 2, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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