Prevalence and causes of acute abdominal pain in adult patients presenting to the emergency department in Aleppo university hospital: a cross-sectional study

ISRCTN ISRCTN15514055
DOI https://doi.org/10.1186/ISRCTN15514055
Submission date
01/11/2024
Registration date
04/11/2024
Last edited
04/11/2024
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Signs and Symptoms
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Background and study aims
This study aims to understand the different causes of sudden abdominal pain in patients who come to the emergency department. We want to find out how common each cause is and how accurate different tests and examinations are in diagnosing these conditions.

Who can participate?
Adults aged 13 years and older who come to the emergency department with sudden abdominal pain can participate in this study. We are not including patients with chronic or unspecified abdominal pain, or those under 13 years old.

What does the study involve?
Participants will be asked to fill out a questionnaire about their symptoms, medical history, and other relevant information. They will also undergo a clinical examination and may have laboratory tests and imaging investigations as part of their routine care. The data collected will help us identify the causes of their abdominal pain and evaluate the accuracy of different diagnostic methods.

What are the possible benefits and risks of participating?
By participating, patients will contribute to improving the understanding and diagnosis of acute abdominal pain, which could benefit future patients. There are no additional risks beyond those associated with the routine medical care they will receive.

Where is the study run from?
Emergency Department of Aleppo University Hospital (Syria)

When is the study starting and how long is it expected to run for?
August 2024 to December 2024

Who is funding the study?
Investigator initiated and funded

Who is the main contact?
Mohammad Al-Jawad, mhammadjawad877@gmail.com

Contact information

Mr Mohammad Al-Jawad
Public, Scientific, Principal Investigator

Aleppo University
Aleppo
-
Syria

ORCiD logoORCID ID 0009-0002-7633-3541
Phone +963 946148173
Email mhammadjawad877@gmail.com

Study information

Study designSingle-center cross-sectional observational study
Primary study designObservational
Secondary study designCross sectional study
Study setting(s)Hospital
Study typeScreening
Participant information sheet No participant information sheet available
Scientific titleUnderstanding acute abdominal pain: a study from Aleppo university hospital
Study acronymPACAP
Study objectivesTo determine the prevalence causes of differential diagnoses for acute abdominal pain in patients presenting to the emergency department.
Ethics approval(s)

Approved 25/08/2024, University of Aleppo Ethics Committee (-, Aleppo, -, Syria; +963 212622301; cmoffice@alepuniv.edu.sy), ref: 2408

Health condition(s) or problem(s) studiedPrevalence and causes of acute abdominal pain in adult patients presenting to the Emergency Department at Aleppo University Hospital
InterventionThis study employs a cross-sectional observational methodology. Adult patients presenting with acute abdominal pain at the Emergency Department of Aleppo University Hospital will be assessed. Data will be collected through structured interviews and clinical examinations. Relevant tests, such as blood tests and imaging studies (e.g., ultrasound), will be performed as deemed necessary by the attending physicians. Observations regarding the patients' demographics, clinical presentations, and final diagnoses will be documented to identify the prevalence and causes of acute abdominal pain.
Intervention typeNot Specified
Primary outcome measureMeasured at a single time point:
1. Prevalence of differential diagnoses for acute abdominal pain is measured using clinical records
2. Most common cause of acute abdominal pain is measured using clinical records
3. Diagnostic accuracy of clinical examination is measured using sensitivity and specificity analysis
4. Diagnostic accuracy of laboratory investigations is measured using sensitivity and specificity analysis
5. Diagnostic accuracy of imaging investigations is measured using sensitivity and specificity analysis
6. Age is measured using a questionnaire
7. Gender is measured using a questionnaire
8. Marital status is measured using a questionnaire
9. Employment status is measured using a questionnaire
10. Location of abdominal pain is measured using a questionnaire
11. Duration of abdominal pain is measured using a questionnaire
12. Nature of abdominal pain is measured using a questionnaire
13. Associated symptoms are measured using a questionnaire
14. Progression of symptoms is measured using a questionnaire
15. Previous treatment for abdominal pain is measured using a questionnaire
16. Abdominal examination findings are measured using clinical examination
17. Radiation of pain is measured using a questionnaire
18. Alleviating or exacerbating factors are measured using a questionnaire
19. Pain score is measured using the NRS scale
20. Impact on daily activities is measured using a questionnaire
21. Significant clinical findings are measured using clinical examination
22. Laboratory test results are measured using laboratory tests
23. Imaging investigation results are measured using imaging tests
24. Final diagnosis is measured using clinical records
Secondary outcome measuresThere are no secondary outcome measures
Overall study start date25/08/2024
Completion date01/12/2024

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit13 Years
Upper age limit100 Years
SexBoth
Target number of participants900
Total final enrolment951
Key inclusion criteria1. Adult patients (aged 13 years and above)
2. Patients with acute abdominal pain
Key exclusion criteria1. Chronic abdominal pain
2. Unspecified abdominal pain
3. Patient under 13 years
Date of first enrolment01/10/2024
Date of final enrolment30/10/2024

Locations

Countries of recruitment

  • Syria

Study participating centre

Aleppo University Hospital
Aleppo
-
Syria

Sponsor information

University of Aleppo
University/education

Aleppo
Aleppo
963
Syria

Phone +963 212622301
Email cmoffice@alepuniv.edu.sy
Website http://www.alepuniv.com/
ROR logo "ROR" https://ror.org/03mzvxz96

Funders

Funder type

Other

Investigator initiated and funded

No information available

Results and Publications

Intention to publish date15/12/2024
Individual participant data (IPD) Intention to shareYes
IPD sharing plan summaryAvailable on request
Publication and dissemination planPlanned publication in a peer-reviewed journal
IPD sharing planThe datasets generated during and/or analysed during the current study will be available upon request from Mohammad Al-Jawad, mhammadjawad877@gmail.com.

Editorial Notes

04/11/2024: Study's existence confirmed by the University of Aleppo Ethics Committee.