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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01853683
Other study ID # 13/02E
Secondary ID
Status Terminated
Phase N/A
First received May 8, 2013
Last updated November 8, 2016
Start date April 2013
Est. completion date April 2016

Study information

Verified date November 2016
Source Children's Hospital of Eastern Ontario
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

Appendicitis is one of the most common surgical problems in children, with 20-35% of patients having perforated by the time they present to a doctor. In these cases, the patient is often treated non-surgically with antibiotics. Once a patient has improved, it is not known whether it is better to perform an interval appendectomy (IA) or to continue a watchful waiting approach. The purpose of this trial is to determine if expectant nonoperative management (watchful waiting) is not inferior compared to IA management after successful conservative treatment of appendiceal mass at admission.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- Under 18 years of age

- Perforated appendicitis where the treating physician chooses to follow the conservative approach rather than performing an immediate appendectomy

Exclusion Criteria:

- Uncertainty about the diagnosis

- The need for laparotomy/laparoscopy for another reason

- Perforated appendicitis with diffuse abdominal fluid on imaging associated with a clinical picture of severe sepsis

- Another medical condition that may affect the decision to operate e.g., inflammatory bowel disease

- A comorbidity or chronic illness that contraindicates the watchful waiting approach, e.g, diabetes or cardiac problems

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Conservative Management

Operative Management


Locations

Country Name City State
Canada Children's Hospital of Eastern Ontario Ottawa Ontario

Sponsors (1)

Lead Sponsor Collaborator
Children's Hospital of Eastern Ontario

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrent appendicitis for the conservative group During a year of follow-up Yes
Primary Operative complications for the operative group During a year of follow-up Yes
Secondary Duration of hospital stay This is the patients' original hospital stay, and re-admission for interval appendectomy when applicable, an expected average of 5 days No
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