Limited Abdominal CT in ED Patients With Abdominal Pain

Abdominal Pain Clinical Trial

— LACTINEDAP  

Official title:

Prospective Study of Z-axis-limited Abdominal CT Guided by Region of Tenderness in the Diagnosis and Management of Adult Emergency Department Patients With Acute Nontraumatic Abdominal Pain and Tenderness

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02146521
• Other study ID #: Pro00050303
• Status: Withdrawn
• Phase: N/A
• First received: May 15, 2014
• Last updated: February 27, 2018
• Start date: November 1, 2017
• Est. completion date: May 2019

Study information

• Verified date: February 2018
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The purpose of the study is to compare the diagnosis and management (treatment and disposition) of adult emergency department patients with acute nontraumatic abdominal pain and tenderness, based on two CT techniques:

1. Standard (complete) abdominal-pelvic CT. The American College of Radiology calls for the cephalad limit of abdominal CT to begin at the dome of the diaphragm, and the caudad limit of pelvic CT to extend through the ischial tuberosities.

2. A z-axis restricted subset of images digitally obtained from the original CT dataset, determined by the region of tenderness identified by the examining emergency physician and marked on the patient prior to the performance of the CT. This z-axis restricted CT does not require any additional radiation exposure to the patient, as it will be produced by computer extraction of data from the original standard abdominal-pelvic CT.

The investigators hypothesize that the diagnosis and management will not differ when guided by the two CT scan interpretations. Radiation doses will be calculated for each of the two techniques.

Description:

This will be a prospective study with informed consent from patient subjects.

Informed consent will be obtained prior to subject enrollment. The study protocol requires the following steps to be performed, each of which is described in more detail later in this document:

1. Potential patient subject is identified by research staff, by virtue of abdominal-pelvic CT being ordered for clinical evaluation of nontraumatic abdominal pain and tenderness, as determined by a board-certified attending emergency physician.

2. Research staff applies inclusion and exclusion criteria to confirm patient eligibility.

3. Potential subjects who fail one or more inclusion or meet one or more exclusion criteria are recorded in electronic research log with reason for exclusion but are not asked to participate in study. Recorded information includes age (if greater than 89, will simply be recorded as "greater than 89"), gender, race/ethnicity, date, and reason for exclusion. No identifiers are recorded for these patients. The purpose of this information is to allow comparison of the enrolled group with all patients with abdominal pain undergoing CT. This will be part of a CONSORT flow diagram, allowing readers to understand potential selection bias and to understand the probable clinical population in the context of all emergency department's (ED) patients undergoing abdominal CT.

4. Eligible potential subjects (meeting all inclusion and no exclusion criteria) are asked to participate in study with informed consent. The study will be introduced to potential subjects by the emergency physician caring for this patient. The study will be introduced only after CT for evaluation of abdominal pain and tenderness is ordered by the physicians caring for the patient, as this is a study inclusion criterion. Potential subjects who do not give informed consent to participate are recorded in electronic research log but not enrolled in study. No identifiers are recorded for these patients. Recorded information includes age (if greater than 89, will simply be recorded as "greater than 89"), gender, race/ethnicity, date, and reason for exclusion. No identifiers are recorded for these patients.

5. Patients who give informed consent are enrolled in study as subjects.

6. Attending board-certified emergency physician places skin surface markers delineating region of abdominal tenderness, using an examination technique described below. Patient is marked with stickers while in supine position with arms above head, as required for CT. Attending board-certified emergency physician also places additional markers to blind radiological interpretation with respect to actual area of tenderness. Attending board-certified emergency physician is also asked to report the working diagnosis, treatment and disposition plan prior to CT scan being performed. An electronic standardized reporting form will be used. Reporting forms are designed in a format of electronic surveys and will be stored on password-protected server, designed specifically for research purposes. The information to be collected will be the same as the information in the attached appendices.

7. Patient undergoes CT scan of complete abdomen and pelvis following usual institutional protocol, concordant with American College of Radiology standard.1

8. Images corresponding to the region of tenderness (z-axis restricted) are loaded onto a server. A board-certified attending radiologist blinded to the remaining CT images interprets the z-axis limited CT images and generates an electronic report, using a standardized research reporting system. The report is electronically time-stamped and cannot be altered.

9. The attending board-certified emergency physician is immediately provided with the electronic CT report from the z-axis limited CT. That physician immediately completes a standardized electronic research reporting form, indicating the current clinical diagnosis, treatment plan, and disposition. The form is electronically time-stamped and cannot be altered.

10. The board-certified attending radiologist who interpreted the z-axis restricted CT is then immediately contacted and interprets the complete CT, including all available images. A report is generated using similar standardized electronic research reporting system used for the z-axis restricted CT. The report is electronically time-stamped and cannot be altered.

11. The attending board-certified emergency physician is immediately provided with the CT report from the complete CT. That physician immediately completes an electronic standardized research reporting form, indicating the current clinical diagnosis, treatment plan, and disposition. The form is electronically time-stamped and cannot be altered.

12. Patient care then proceeds according to the usual clinical standard in the institution.

13. Subject records are reviewed to determine final diagnosis and treatment.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: May 2019
• Est. primary completion date: May 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• emergency department's patients undergoing CT evaluation for acute abdominal pain and tenderness (acute is defined as onset of current episode within 7 days of emergency department presentation).

Exclusion Criteria:

• neurological disorders

• altered mental status

• history of intra-abdominal surgery in the past 30 days

• BMI higher than 35

• immunocompromised patients

• abdominal trauma in the past 30 days

• CT is ordered for the following indications:

• isolated vomiting

• fever without source

• staging of malignancy

• isolated flank pain or suspected renal colic

Related Conditions & MeSH terms

• Abdominal Pain

Locations

Country	Name	City	State
United States	Duke University Medical Center	Durham	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Duke University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Diagnosis, treatment and disposition	The diagnosis, treatment, and disposition plans based on the z-axis restricted CT and the full CT will be compared for agreement.	Records will be reviewed from the ED visit date to the date of discharge from the hospital or up to 30 days following ED visit, whichever comes last
Secondary	radiation reduction	The radiation doses resulting from a z-axis restricted CT and the full CT will be compared using dose-length products.	Records will be reviewed 30 days after the ED visit or date of discharge from the hospital, whichever comes first