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Operative Versus Non-Operative Management for Appendicitis With Abscess or Phlegmon

Primary Purpose

Appendicitis

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Operative management
Drainage or antibiotics
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Appendicitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

1. Complicated appendicitis with presumed perforation on (computer tomography) CT scan AND phlegmon or abscess greater than 2 centimeter (cm).

Exclusion Criteria:

  1. Antibiotic therapy greater than 24 hours prior to considering for enrollment.
  2. Attempted drainage before randomization
  3. Pregnancy
  4. Antibiotic allergy requiring the use of something other than a beta-lactam or quinolone based therapy.
  5. Previous major intra-abdominal surgery by laparotomy
  6. Hospitalization within 2 weeks of randomization
  7. Presence of septic shock on admission.
  8. Mechanical ventilation
  9. Acute renal failure requiring dialysis

Sites / Locations

  • Yale New Haven HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Surgery

Non-operative management

Arm Description

Patients who choose operations will have surgery performed to remove the appendix laparoscopically, through 3 or 4 small incisions. All patients in the operative group will receive standard perioperative antibiotics. They will also have the abscess(es) drained during the same surgery if there is one present. In some cases, the operation may be too difficult to perform laparoscopically, so an open appendectomy will be performed, involving a longer incision to remove the appendix. In some cases, both laparoscopic and open are performed. The surgeon may also choose to remove a section of the intestine with the appendix or perform additional procedures.

If a patient chooses non-operative management and if an abscess is present and amenable to percutaneous drainage this will be performed. If there is no abscess or it is not amenable to drainage antibiotics alone will be provided.

Outcomes

Primary Outcome Measures

Number of hospital days
This includes all hospital days during the initial stay and any readmission.

Secondary Outcome Measures

Need for additional intervention for appendicitis
Percutaneous drainage, unplanned operative intervention.
Intra-abdominal abscess
Failed attempted procedure.
Conversion from laparoscopic to open surgery, conversion from non-operative to operative management, percutaneous drainage not possible or unsuccessful.
Complications
Defined by National Surgical Quality Improvement Program criteria.
Number of interventions for abscess
Need for bowel resection.
Need for bowel resection
Occurrence of delayed appendectomy
Recurrence
Presence of malignancy in any resected specimen
Days of disability
Days away from work or school.
Gastrointestinal (GI) quality of life
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.
GI quality of life
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.
GI quality of life
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.

Full Information

First Posted
November 16, 2019
Last Updated
October 23, 2023
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT04168866
Brief Title
Operative Versus Non-Operative Management for Appendicitis With Abscess or Phlegmon
Official Title
Operative Versus Non-Operative Management for Appendicitis With Abscess or Phlegmon
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 11, 2020 (Actual)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University

4. Oversight

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

5. Study Description

Brief Summary
The investigators aim to determine if early operative intervention is superior to non-operative management for adult patients with computerized tomography (CT)-proven complicated appendicitis with phlegmon or abscess.
Detailed Description
Complicated appendicitis with abscess or phlegmon represents a challenging problem to emergency general surgeons, and the preferred treatment remains controversial. A variety of therapies have been recommended including early operative intervention, delayed operative intervention, and non-operative management. Recently, a prospective randomized controlled trial from a single center was conducted in Finland comparing operative and non-operative management of appendiceal abscess. Patients managed in the operative arm were found to have a shorter length of stay, fewer re-admissions, and fewer additional interventions than those managed in the non-operative group, but there is no high-quality randomized control trial conducted in the United States to support this. The investigators, therefore plan to carry out a multi-center, patient choice study comparing operative and non-operative management of complicated appendicitis with abscess or phlegmon in the United States.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Appendicitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Surgery
Arm Type
Experimental
Arm Description
Patients who choose operations will have surgery performed to remove the appendix laparoscopically, through 3 or 4 small incisions. All patients in the operative group will receive standard perioperative antibiotics. They will also have the abscess(es) drained during the same surgery if there is one present. In some cases, the operation may be too difficult to perform laparoscopically, so an open appendectomy will be performed, involving a longer incision to remove the appendix. In some cases, both laparoscopic and open are performed. The surgeon may also choose to remove a section of the intestine with the appendix or perform additional procedures.
Arm Title
Non-operative management
Arm Type
Active Comparator
Arm Description
If a patient chooses non-operative management and if an abscess is present and amenable to percutaneous drainage this will be performed. If there is no abscess or it is not amenable to drainage antibiotics alone will be provided.
Intervention Type
Procedure
Intervention Name(s)
Operative management
Intervention Description
Surgery for computer tomography (CT)-proven complicated appendicitis with phlegmon or abscess.
Intervention Type
Other
Intervention Name(s)
Drainage or antibiotics
Intervention Description
If an abscess is present and amenable to percutaneous drainage this will be performed. If there is no abscess or it is not amenable to drainage antibiotics alone will be provided.
Primary Outcome Measure Information:
Title
Number of hospital days
Description
This includes all hospital days during the initial stay and any readmission.
Time Frame
Within 60 days of randomization.
Secondary Outcome Measure Information:
Title
Need for additional intervention for appendicitis
Description
Percutaneous drainage, unplanned operative intervention.
Time Frame
Within one year of the index admission.
Title
Intra-abdominal abscess
Time Frame
More than 7 days after index admission but within 60 days of randomization.
Title
Failed attempted procedure.
Description
Conversion from laparoscopic to open surgery, conversion from non-operative to operative management, percutaneous drainage not possible or unsuccessful.
Time Frame
Within 60 days of randomization.
Title
Complications
Description
Defined by National Surgical Quality Improvement Program criteria.
Time Frame
Within 60 days of randomization.
Title
Number of interventions for abscess
Time Frame
Within 60 days of randomization.
Title
Need for bowel resection.
Time Frame
Within 60 days of randomization.
Title
Need for bowel resection
Time Frame
Within 60 days of randomization.
Title
Occurrence of delayed appendectomy
Time Frame
Within one year of index admission.
Title
Recurrence
Time Frame
Within one year of index admission.
Title
Presence of malignancy in any resected specimen
Time Frame
Within one year of index admission.
Title
Days of disability
Description
Days away from work or school.
Time Frame
Within 60 days of randomization.
Title
Gastrointestinal (GI) quality of life
Description
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.
Time Frame
30 days after randomization.
Title
GI quality of life
Description
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.
Time Frame
60 days after randomization.
Title
GI quality of life
Description
This outcome will be measured by the Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptoms Scale. This scale includes 8 subscales of which the investigators will use 6 for a maximum of 41 items, though usually less due to skip logic. Each item is measured on a 5-point scale. Items are summed by subscale and converted to a final score by a computer algorithm. A higher score indicates greater symptom severity and lower quality of life.
Time Frame
One year after randomization.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Complicated appendicitis with presumed perforation on (computer tomography) CT scan AND phlegmon or abscess greater than 2 centimeter (cm). Exclusion Criteria: Antibiotic therapy greater than 24 hours prior to considering for enrollment. Attempted drainage before randomization Pregnancy Antibiotic allergy requiring the use of something other than a beta-lactam or quinolone based therapy. Previous major intra-abdominal surgery by laparotomy Hospitalization within 2 weeks of randomization Presence of septic shock on admission. Mechanical ventilation Acute renal failure requiring dialysis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kevin Schuster, MD, MPH
Phone
203 785 2572
Email
kevin.schuster@yale.edu
Facility Information:
Facility Name
Yale New Haven Hospital
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06512
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kevin Schuster, MD
Phone
203-785-2572
Email
kevin.schuster@yale.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25775072
Citation
Mentula P, Sammalkorpi H, Leppaniemi A. Laparoscopic Surgery or Conservative Treatment for Appendiceal Abscess in Adults? A Randomized Controlled Trial. Ann Surg. 2015 Aug;262(2):237-42. doi: 10.1097/SLA.0000000000001200.
Results Reference
background

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Operative Versus Non-Operative Management for Appendicitis With Abscess or Phlegmon

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