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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00935207
Other study ID # 2009-0054
Secondary ID
Status Terminated
Phase N/A
First received June 17, 2009
Last updated May 2, 2013
Start date June 2009
Est. completion date December 2011

Study information

Verified date May 2013
Source University of Mississippi Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to show the impact of a pain diary on the communication of pain by pediatric patients. Participants will be given a pain diary after consent and asked to complete the record each time they have pain. A survey about the efficacy of the pain diary will be taken prior to discharge by the nurse, physician, patient and parents. The hypothesis is that the pain diary will improve the communication.


Recruitment information / eligibility

Status Terminated
Enrollment 8
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 3 Years to 19 Years
Eligibility Inclusion Criteria:

- Inpatients at the Blair E. Batson Hospital for Children 3-19 years of age, receiving regular controlled substance analgesic defined as: codeine with acetaminophen, fentanyl, hydromorphone, meperidine, morphine, oxycodone with acetaminophen, propoxyphene with acetaminophen, and hydrocodone with acetaminophen.

Exclusion Criteria:

- Admitted to the Pediatric Intensive Care Unit

- Surgical patients, defined as patients having surgery since admission other than minor procedures

- Patients anticipated to receive pain medication for less than 24 hours

- Patients unable to verbally communicate their pain

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Pediatric Pain Diary
Pain diary designed for pediatric patients

Locations

Country Name City State
United States University of Mississippi Medical Center Jackson Mississippi

Sponsors (1)

Lead Sponsor Collaborator
University of Mississippi Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Child Survey Hospital discharge No
Primary Parent Survey Hospital Discharge No
Primary Nurse Survey Hospital Discharge No
Primary Physician Survey Hospital Discharge No
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