Finding Evidence to Treat Or Reassure in Appendicitis (FETOR)
FETOR
1 other identifier
interventional
58
1 country
1
Brief Summary
Acute appendicitis is the most common surgical emergency in childhood. Despite access to current diagnostic modalities, diagnosis may be challenging since the child may have difficulty in articulating symptoms. Additionally there is a high frequency of atypical presentation and rapid progression. Delayed diagnosis in children is reported as being up to 60%. Delayed diagnosis \>48hr increases the perforation rate from 21% to 71%. Around 20% of children presenting with appendicitis have perforated by the time they come to surgery. Appendix perforation is associated with a prolonged hospital stay and increased cost. Once perforated, major complication rates increase from 1.2% to 6.4%, median bed stay increases from 2 to 6 days and hospitalisation costs are estimated at US $33,348. Conversely, a false positive diagnosis leads to unnecessary surgery in 12%. It has been suggested that only 35% of surgical referrals with possible appendicitis actually need surgery thus impacting on resource use. A reliable test, especially if painless, would be very useful. If positive the child could undergo early appendicectomy in expectation of a reduction in the perforation rate (and, therefore, reduction in hospital stay). If negative the child could be discharged home safely. No adequate biomarker has been identified. Technology already exists to detect changes in Volatile Organic Compounds (VOC) in gases. VOC analysis is already used commercially to identify disease processes in animals and crops. Although VOC has been previously used to detect human diseases, it has never been used to look for changes in the composition of breath in appendicitis. The investigators hypothesise that the composition of VOC's in children with appendicitis will differ from those without. The investigators anticipate these differences will be of diagnostic and prognostic value in clinical practice. The feasibility of collecting breath samples from children with possible appendicitis to allow VOC testing has not been examined.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Aug 2017
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 4, 2017
CompletedFirst Posted
Study publicly available on registry
August 14, 2017
CompletedStudy Start
First participant enrolled
August 30, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 9, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2019
CompletedNovember 5, 2019
November 1, 2019
2 years
July 4, 2017
November 4, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Breath collection for analysis
Collect breath from children with abdominal pain meeting inclusion criteria assess ment to changes in Volatile Organic Compounds (VOC)
3 minutes
Study Arms (1)
Patients with suspected appendicitis
EXPERIMENTALPatients with suspected appendicitis Aged 5 and up to their 16th birthday on arrival to A\&E
Interventions
Blowing into the mouthpiece of diagnostic device
Eligibility Criteria
You may qualify if:
- Patients with suspected appendicitis
- Aged 5 and up to their 16th birthday on arrival to A\&E
- Patients referred to the Paediatric surgical team that have presented to the Leeds General Infirmary through A\&E, the Children's Assessment Unit, or via direct referral from another team or hospital.
- Consecutive presentations who can have some or all of VOC sampling during working week.
You may not qualify if:
- Patients with known alternative cause of abdominal pain (e.g. known Inflammatory Bowel Disease)
- Patients who are both admitted and discharged when no researcher is available
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Leeds Teaching Hospitals NHS Trust
Leeds, United Kingdom
Related Publications (1)
Wong DC, Relton SD, Lane V, Ismail M, Goss V, Bytheway J, West RM, Deuchars J, Sutcliffe J. Bedside breath tests in children with abdominal pain: a prospective pilot feasibility study. Pilot Feasibility Stud. 2019 Nov 5;5:121. doi: 10.1186/s40814-019-0502-x. eCollection 2019.
PMID: 31720000DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 4, 2017
First Posted
August 14, 2017
Study Start
August 30, 2017
Primary Completion
September 9, 2019
Study Completion
September 30, 2019
Last Updated
November 5, 2019
Record last verified: 2019-11