Pain Quantification and Pain Management in Interventional Radiology (IR)

NCT00500942 | Completed

• 1 other identifier: ID02-374
• Study Type: observational
• Target: 374
• Locations: 1 country
• Sites: 1

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).

Conditions

Pain

Keywords

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

Outcome Measures

Primary Outcomes (1)

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

  6 Years

Secondary Outcomes (1)

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

  6 Years

Study Arms (1)

1

Patients having a standard procedure performed in Interventional Radiology.

Behavioral: Questionnaire

Interventions

Questionnaire BEHAVIORAL

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

Also known as: Survey

1

Eligibility Criteria

• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients having a standard procedure performed in Interventional Radiology.

You may qualify if:

• 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

You may not qualify if:

• 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

Sponsors & Collaborators

• M.D. Anderson Cancer Center: lead

Study Sites (1)

U.T.M.D. Anderson Cancer Center

Houston, Texas, 77030, United States

Location

Related Links

• MD Anderson Cancer Center

MeSH Terms

Conditions

Pain; Agnosia; Patient Satisfaction

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms; Perceptual Disorders; Neurobehavioral Manifestations; Nervous System Diseases; Treatment Adherence and Compliance; Health Behavior; Behavior

Intervention Hierarchy (Ancestors)

Data Collection; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Public Health; Environment and Public Health

Study Officials

• Prachee Singh, BS

  M.D. Anderson Cancer Center

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE ONLY
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 12, 2007
• First Posted: July 13, 2007
• Study Start: January 1, 2003
• Primary Completion: June 1, 2009
• Study Completion: June 1, 2009
• Last Updated: August 2, 2012

Record last verified: 2012-08

Locations

US (1)