NCT03248102

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Aug 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
1 month until next milestone

First Posted

Study publicly available on registry

August 14, 2017

Completed
16 days until next milestone

Study Start

First participant enrolled

August 30, 2017

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 9, 2019

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2019

Completed
Last Updated

November 5, 2019

Status Verified

November 1, 2019

Enrollment Period

2 years

First QC Date

July 4, 2017

Last Update Submit

November 4, 2019

Conditions

Keywords

paediatric

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

EXPERIMENTAL

Patients with suspected appendicitis Aged 5 and up to their 16th birthday on arrival to A\&E

Diagnostic Test: Blowing into the mouthpiece

Interventions

Blowing into the mouthpiece of diagnostic device

Patients with suspected appendicitis

Eligibility Criteria

Age5 Years - 16 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17)

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

Location

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.

MeSH Terms

Conditions

Appendicitis

Condition Hierarchy (Ancestors)

Intraabdominal InfectionsInfectionsGastroenteritisGastrointestinal DiseasesDigestive System DiseasesCecal DiseasesIntestinal Diseases

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

Locations