Antibiotic Instillation in Appendicitis
Primary Purpose
Complicated Appendicitis, Acute Appendicitis
Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Ceftriaxone
Intra-peritoneal Fluid Aspiration
Sponsored by
About this trial
This is an interventional treatment trial for Complicated Appendicitis
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with acute appendicitis and are scheduled to undergo urgent appendectomy
- Between 3-18 years of age at time of appendectomy
- Has intraoperative findings of complex appendicitis defined by: visible hole in the appendix, extra-luminal fecalith, diffuse fibropurulent exudate outside the RLQ/pelvis, or intraperitoneal abscess
- Weighs over 20kg at time of surgery
Exclusion Criteria:
- Pregnant
- Has a penicillin or cephalosporin allergy that is severe or anaphylactic in nature, prohibiting the use of these antibiotics
- Has simple appendicitis
- Undergoes appendectomy following failed or planned medical management of appendicitis
Sites / Locations
- Johns Hopkins All Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Standard of Care (Arm A)
Standard of Care and Antibiotic instillation (Arm B)
Arm Description
Intra-operative aspiration of intra-peritoneal fluid after successful appendectomy.
Intra-operative aspiration of intra-peritoneal fluid after successful appendectomy and subsequent instillation of 10ml of intra-peritoneal ceftriaxone (2g)
Outcomes
Primary Outcome Measures
Feasibility of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Percentage of Eligible Participants Who Agree to Participate
The study will be deemed feasible if >50% of potential participants agree to participate. This benchmark is based on a previous similar study completed in this population.
Feasibility of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Percentage of Eligible Participants Who Complete All Intervention Sessions and Measurement Time Points
The study will be deemed feasible if at least 75% of potential participants complete all intervention sessions and measurement time points per study protocol. This benchmark is based on a previous similar study completed in this population.
Safety of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Number of Adverse Events
Safety will be determined by adverse events associated with the use of intra-peritoneal antibiotic instillation for the treatment of peritonitis caused by complex appendicitis.
Secondary Outcome Measures
Full Information
NCT ID
NCT05470517
First Posted
July 19, 2022
Last Updated
August 28, 2023
Sponsor
Johns Hopkins All Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05470517
Brief Title
Antibiotic Instillation in Appendicitis
Official Title
Antibiotic Instillation in Acute Complex Appendicitis for Prevention of Deep Space Surgical Site Infections
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 5, 2023 (Actual)
Primary Completion Date
March 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Johns Hopkins All Children's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
5. Study Description
Brief Summary
Appendicitis (inflammation of the wall of the appendix, causing pain and tenderness in the abdomen) has a range of severity that goes from simple to complicated. Complicated appendicitis may present with infected fluid inside of the abdomen or a perforation or hole in the intestines.
This research is being done to determine if placing an antibiotic solution in the abdomen at the time the appendix is removed is a safe procedure in patients between the ages of 3 and 18 years old with findings of complicated appendicitis.
Johns Hopkins All Children's Hospital (JHACH)'s current standard of care for patients with complicated appendicitis includes suctioning the infected fluid out of the abdomen at the time the appendix is removed. As part of this study, the investigators would like to see if patients with complicated appendicitis will benefit from routine care plus leaving an antibiotic solution inside the abdomen, after fully suctioning the infected fluid out of the abdomen.
Detailed Description
Appendicitis is one of the most common surgical diagnoses in the pediatric population and the most common surgical emergency in children. In complex appendicitis, the sequelae have progressed beyond the confines of the organ, and have led to purulent fluid in the intra-abdominal space, spillage of intestinal contents, or gross perforation of the appendix. Complicated appendicitis occurs in up to 20% of cases and is associated with a much higher morbidity and mortality. Previous studies have shown that local treatment of peritonitis associated with peritoneal dialysis (PD) catheters with intra-peritoneal antibiotics has had significant improvement of outcomes. The intra-peritoneal route is preferable as compared to oral and intravenous antibiotic administration due to elevated local levels of the antibiotic above the minimum inhibitory concentration while avoiding venipuncture and systemic side effects. There is minimal risk associated with involvement in this study given that the investigators will be screening for any history of allergies to penicillin or cephalosporins, and excluding these patients. Ceftriaxone is commercially available, has a low risk profile, and is generally well tolerated with minimal side effects.
The investigators' treatment period will include a one-time intra-operative dose of intra-peritoneal ceftriaxone (or an appropriate second or third generation cephalosporin to be designated at the discretion of the institutional Antibiotic Stewardship committee should ceftriaxone be unavailable). Typical dosing strategies for intra-peritoneal ceftriaxone administration occur on a daily basis, so the investigators' treatment period will also include the 24 hours following intra-peritoneal administration of ceftriaxone. All patients diagnosed with acute complicated appendicitis intra-operatively, and entered into the investigators' study, will also receive a minimum 48 hours of intravenous antibiotics as an inpatient, allowing for continued observation. The investigators will be treating pediatric patients who are intra-operatively diagnosed with complex appendicitis, as defined by any of the following: visible hole in the appendix, extra-luminal fecalith, diffuse fibropurulent exudate outside the right lower quadrant (RLQ)/pelvis, or intraperitoneal abscess. All patients will have been admitted to Johns Hopkins All Children's Hospital with a diagnosis of acute appendicitis prior to surgical intervention. Patients will then be randomized once diagnosed with complex appendicitis intra-operatively. Patients with allergies to penicillin or cephalosporins will be excluded pre-operatively, as well as patients who do not meet the weight requirement, are pregnant, being treated non-operatively, and those who have been intra-operatively diagnosed with simple appendicitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Complicated Appendicitis, Acute Appendicitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Single-blinded randomized controlled pilot phase 2 study
Masking
Participant
Masking Description
The surgeon and team administering the treatment will not be blinded; however, patients, patients' families, and hospital caregivers outside of the operating room will be blinded to the treatment.
Allocation
Randomized
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Standard of Care (Arm A)
Arm Type
Active Comparator
Arm Description
Intra-operative aspiration of intra-peritoneal fluid after successful appendectomy.
Arm Title
Standard of Care and Antibiotic instillation (Arm B)
Arm Type
Experimental
Arm Description
Intra-operative aspiration of intra-peritoneal fluid after successful appendectomy and subsequent instillation of 10ml of intra-peritoneal ceftriaxone (2g)
Intervention Type
Drug
Intervention Name(s)
Ceftriaxone
Other Intervention Name(s)
Ceftriaxone sodium
Intervention Description
Ceftriaxone is a sterile, semisynthetic, broad-spectrum cephalosporin antibiotic for intravenous, intramuscular, or intra-peritoneal administration.
Ceftriaxone is a white powder, which is soluble in water. In this study ceftriaxone crystalline powder will be dissolved in 0.9% sodium chloride solution prior to intra-peritoneal instillation.
Antibiotic instillation will be introduced into the RLQ/pelvis after the appendectomy is completed and all intra-peritoneal fluid is aspirated. Ceftriaxone solution will be used depending on availability and pharmacy stock for use at Johns Hopkins All Children's Hospital. The ceftriaxone powder (2g) will be dissolved in 9ml of sterile normal saline, for a total instillation volume of 10ml. This fluid will then be instilled and left to dwell in the area of the peritoneal cavity where the appendix was removed.
Intervention Type
Procedure
Intervention Name(s)
Intra-peritoneal Fluid Aspiration
Intervention Description
Intra-operative aspiration of intra-peritoneal fluid after successful appendectomy.
Primary Outcome Measure Information:
Title
Feasibility of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Percentage of Eligible Participants Who Agree to Participate
Description
The study will be deemed feasible if >50% of potential participants agree to participate. This benchmark is based on a previous similar study completed in this population.
Time Frame
Up to 30 days postoperatively
Title
Feasibility of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Percentage of Eligible Participants Who Complete All Intervention Sessions and Measurement Time Points
Description
The study will be deemed feasible if at least 75% of potential participants complete all intervention sessions and measurement time points per study protocol. This benchmark is based on a previous similar study completed in this population.
Time Frame
Up to 30 days postoperatively
Title
Safety of the Use of Antibiotic Solution Instillation Following Intraoperative Diagnosis of Complex Appendicitis as Assessed by Number of Adverse Events
Description
Safety will be determined by adverse events associated with the use of intra-peritoneal antibiotic instillation for the treatment of peritonitis caused by complex appendicitis.
Time Frame
Up to 30 days postoperatively
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed with acute appendicitis and are scheduled to undergo urgent appendectomy
Between 3-18 years of age at time of appendectomy
Has intraoperative findings of complex appendicitis defined by: visible hole in the appendix, extra-luminal fecalith, diffuse fibropurulent exudate outside the RLQ/pelvis, or intraperitoneal abscess
Weighs over 20kg at time of surgery
Exclusion Criteria:
Pregnant
Has a penicillin or cephalosporin allergy that is severe or anaphylactic in nature, prohibiting the use of these antibiotics
Has simple appendicitis
Undergoes appendectomy following failed or planned medical management of appendicitis
Has impaired renal function (CrCl <15mL/min)
Has history of neurological conditions such as encephalopathy, seizures, myoclonus and non-convulsive status epilepticus
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
JoAnn DeRosa, RN
Phone
727-767-2941
Email
joann.derosa@jhmi.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Alyssa Green, MD
Email
agree185@jh.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole M. Chandler, MD
Organizational Affiliation
Johns Hopkins All Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins All Children's Hospital
City
Saint Petersburg
State/Province
Florida
ZIP/Postal Code
33701
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicole Chandler, MD
Email
nicole.chandler@jhmi.edu
First Name & Middle Initial & Last Name & Degree
JoAnn DeRosa, RN
Email
joann.derosa@jhmi.edu
12. IPD Sharing Statement
Learn more about this trial
Antibiotic Instillation in Appendicitis
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