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Urinary 5-HIAA for Diagnosis of Acute Appendicitis in Children, Does it Help?

Primary Purpose

Diagnosis of Acute Appendicitis in Children

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
measurement of urinary 5-HIAA
Sponsored by
Tanta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Diagnosis of Acute Appendicitis in Children focused on measuring appendicitis, children, 5-HIAA, scoring systems

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • all children with suspected acute appendicitis

Exclusion Criteria:

  • children received drugs that may affect normal values of urinary 5-HIAA as mono mono oxidase inhibitors

Sites / Locations

  • Tanta University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

group A

group B

Arm Description

subjected to institutional protocol of diagnosis of acute appendicitis

subjected to institutional protocol of diagnosis of acute appendicitis plus measurement of urinary 5-HIAA

Outcomes

Primary Outcome Measures

accurate diagnosis of acute appendicitis in children
number of cases that have been diagnosed as having acute appendicitis
decreasing incidence of negative appendectomy
number of cases that are not appendicitis and not operated
decreasing number of readmitted cases with diagnosis of acute appendicitis
number of cases that had been readmitted with diagnosis of acute appendicitis in both groups

Secondary Outcome Measures

Full Information

First Posted
August 22, 2020
Last Updated
August 25, 2020
Sponsor
Tanta University
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1. Study Identification

Unique Protocol Identification Number
NCT04527263
Brief Title
Urinary 5-HIAA for Diagnosis of Acute Appendicitis in Children, Does it Help?
Official Title
BUILDING UP A DIAGNOSTIC MODEL OF ACUTE APPENDICITIS IN CHILDREN USING URINARY 5-HYDROXY INDOL ACETIC ACID
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
July 2, 2017 (Actual)
Primary Completion Date
July 1, 2020 (Actual)
Study Completion Date
July 2, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tanta University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
it is randomized control study. two groups of children (n=191) were divided into two groups A and B. Group A included children subjected to the classical protocol of diagnosis of acute appendicitis. this protocol consisted of pediatric appendicitis score evaluation, pelvi abdominal ultrasound and measurement of serum CRP. Group B, children had the same previous assessment plus measurement of urinary 5-HIAA.
Detailed Description
1.1- Study design: Patients were randomly categorized into two groups A and B. Randomization was achieved using closed envelop method. Group A (n= 95) included patients that were evaluated using our institutional protocol. This protocol consists of assessment of children using PAS, ultrasound of abdomen and pelvis and serum levels of C-reactive protein. Group B (n= 96) included children that were evaluated by our institutional protocol. In addition, all children gave a mid- stream urine sample for spot urinary 5-HIAA detection. Detailed history was taken. This mainly was to exclude cases with history of foods or drugs that may affect level of serotonin in urine such as mono amino oxidase inhibitors. All related clinical data and laboratory investigations were recorded. 1.2- Quantitation of urinary 5-HIAA level: From each participant, a random urine sample was obtained to assess the urinary 5-HIAA level using a solid phase competitive enzyme-linked immunosorbent assay (ELISA) technique. The commercial kit was purchased and provided by LDN, DN Labor Diagnosika Nord GmbH & Co. Nordhorn, Germany; Catalog #: BA E-1900. As stated by the manufacturer, the urine samples were methylated to derivatize the 5-HIAA. On the provided microtitre plate, the methylated standards, controls and samples are added. 5-HIAA antiserum was then added and incubated for 1 hour. After equilibration, excess free antigen and antigen-antibody complexes are washed out. The affixed bounded antibodies to the solid phase were detected by an anti-rabbit IgG-peroxidase conjugate using TMB as a substrate. The reaction is measured on a microplate reader (Tecan Spectra II, Switzerland), at 450 nm. Quantification of unknown sample concentration is processed by drawing a standard curve with known standard concentrations. The results of 5-HIAA were divided by urinary creatinine and expressed as mg/g creatinine. The inter-assay and intra-assay coefficient of variation were 10.8% and 8.6% respectively. 1.3- Clinical outcome: Diagnosis of acute appendicitis was confirmed by histopathological examination of resected appendix. According to operative findings and pathological reports, the condition ranged from negative appendix to different types of acute appendicitis (catarrhal, suppurative, perforated or gangrenous). Children did not full filling the requirements for diagnosis as acute appendicitis were discharged on symptomatic treatment or after referral to pediatric emergency department. Readmitted cases were recorded. 1.4- Statistical analysis: Statistical analysis was done using IBM SPSS V. 24 (IBM, NY, USA). A descriptive analysis was obtained for patients included in the study. Shapiro-Wilk test was conducted to check for normal distribution of dependent variables, such as urinary 5-HIAA, CRP and histopathological findings. X2 test was used to compare the categorical data. Student T-test was used to compare the normally distributed variable between two groups. Mann-Whitney U test and Kruskal-Wallis test were used for comparing the non-normally distributed variables of two and more than two groups, respectively. Binary logistic regression was performed to determine the independent predictors for acute appendicitis and to combine 5-HIAA and PAS results in both groups. Pearson correlation was used for correlating the urinary 5-HIAA with other acute appendicitis predictors. Receiver operating characteristic (ROC) curve was constructed to assess the diagnostic efficacy of acute appendicitis predictors. The optimal cutoff value for each predictor was assessed via the Youden index. The value of AUC ranged from 0.5 to 1.0. The ability of a diagnostic test to identify patients with appendicitis was considered optimal as AUC value reached closer to 1.0. P-value <0.05 was considered significant

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diagnosis of Acute Appendicitis in Children
Keywords
appendicitis, children, 5-HIAA, scoring systems

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
191 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group A
Arm Type
Active Comparator
Arm Description
subjected to institutional protocol of diagnosis of acute appendicitis
Arm Title
group B
Arm Type
Active Comparator
Arm Description
subjected to institutional protocol of diagnosis of acute appendicitis plus measurement of urinary 5-HIAA
Intervention Type
Diagnostic Test
Intervention Name(s)
measurement of urinary 5-HIAA
Intervention Description
urinary assessment of 5-HIAA
Primary Outcome Measure Information:
Title
accurate diagnosis of acute appendicitis in children
Description
number of cases that have been diagnosed as having acute appendicitis
Time Frame
1 day
Title
decreasing incidence of negative appendectomy
Description
number of cases that are not appendicitis and not operated
Time Frame
1 day
Title
decreasing number of readmitted cases with diagnosis of acute appendicitis
Description
number of cases that had been readmitted with diagnosis of acute appendicitis in both groups
Time Frame
3 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: all children with suspected acute appendicitis Exclusion Criteria: children received drugs that may affect normal values of urinary 5-HIAA as mono mono oxidase inhibitors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammad G Mohammad
Organizational Affiliation
Tanta University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tanta University
City
Tanta
State/Province
Gharbeya
ZIP/Postal Code
31111
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Urinary 5-HIAA for Diagnosis of Acute Appendicitis in Children, Does it Help?

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