MUD: Outpatient Treatment of Uncomplicated Diverticulitis With Either Antibiotic or Nonantibiotic Treatment

Sponsor
Jewish General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03146091
Collaborator
(none)
33
1
2
43.4
0.8

Study Details

Study Description

Brief Summary

Uncomplicated sigmoid diverticulitis is a common disease in Western countries. Traditional management includes inpatient administration of either oral or intravenous antibiotics with resumption of oral intake as symptoms improve. Recent literature has however questioned both inpatient and antibiotic treatment. Indeed, both inpatient and antibiotic treatment are associated with non-negligible risks to patients. The aim of this trial is to assess the feasibility of a randomized controlled trial designed to determine whether nonantibiotic treatment of uncomplicated diverticulitis is safe in the outpatient setting.

Condition or Disease Intervention/Treatment Phase
  • Other: Nonantibiotic treatment of uncomplicated diverticulitis
  • Other: Antibiotic treatment of uncomplicated diverticulitis
N/A

Detailed Description

Uncomplicated sigmoid diverticulitis is a common disease in Western countries. Traditional management includes inpatient administration of either oral or intravenous antibiotics with resumption of oral intake as symptoms improve. Recent literature has however questioned both inpatient and antibiotic treatment. Indeed, both inpatient and antibiotic treatment are associated with non-negligible risks to patients. The aim of this trial is to assess the feasibility of a randomized controlled trial designed to determine whether nonantibiotic treatment of uncomplicated diverticulitis is safe in the outpatient setting. It is designed as a pilot non-inferiority blinded randomized controlled trial. The estimated length of this pilot trial is 1 year. The target population is capable adults of who have a CT-diagnosed episode of uncomplicated diverticulitis who present to the Jewish General Hospital Emergency room.

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Study on Outpatient Treatment of Uncomplicated Diverticulitis With Either Antibiotic or Nonantibiotic Treatment: a Randomized Pilot Trial
Actual Study Start Date :
May 20, 2017
Actual Primary Completion Date :
Dec 30, 2019
Actual Study Completion Date :
Dec 30, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Outpatient nonantibiotic treatment

Other: Nonantibiotic treatment of uncomplicated diverticulitis
Patients randomized to this arm will be treated without antibiotics in the outpatient setting. Pain will be managed with appropriate analgesia as per protocol.

Active Comparator: Outpatient antibiotic treatment

Other: Antibiotic treatment of uncomplicated diverticulitis
Patients randomized to this arm will be treated with antibiotics in the outpatient setting. Pain will be managed with appropriate analgesia as per protocol.

Outcome Measures

Primary Outcome Measures

  1. Participants' retention rate as assessed by the number of participants retained in the study from screening to the end of follow-up. [1 year]

    The primary outcome pertains to the feasibility of a non-inferiority randomized controlled trial. The study group's main concern is that accrual will be impeded by the important change in clinical management that nonantibiotic treatment of uncomplicated diverticulitis requires. Also, the study group is concerned that patients may be lost to follow-up. For these reasons, the primary outcome is the retention rate of patients from screening to the end of follow-up. The rate will be calculated according to (1) the proportion of participants screened but not randomized, and (2) the proportion of participants lost to follow-up.

Secondary Outcome Measures

  1. Treatment failure [1 year]

    Treatment failure is defined as persistence, increase or recurrence of abdominal pain and/or fever, inflammatory bowel obstruction, need for radiological abscess drainage or immediate surgery due to complicated diverticulitis, need for hospital admission, and mortality during the first 60 days after discharge.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age ≥ 18 and < 90 years old

  2. Capable of giving informed consent

  3. Lower abdominal pain and/or tenderness

  4. Confirmed affection of left colon, including descending and sigmoid colon

  5. Confirmed episode of acute uncomplicated diverticulitis on computed tomography (CT) scan defined as wall edema with or without fat stranding. Limited pericolic air with bubbles less than 5 mm in size, and less than 5cm from the colon wall, will be included as uncomplicated diverticulitis. Scan must be performed prior to enrollment and assessment for illegibility. The initial scan is not a study-specific procedure.

Exclusion Criteria:
  1. CT scan shows complicated diverticulitis as defined by the presence of intraperitoneal free perforation (i.e. intraperitoneal contrast extravasation if intra-rectal contrast given, free air under diaphragms, disseminated intraperitoneal air), abscess, obstruction, fistulisation, and phlegmon.

  2. Suspicion of colorectal cancer on CT scan

  3. Immunosuppression (including but not exclusively insulin-dependent diabetes mellitus, chronic liver disease, ongoing chemotherapy, chronic renal failure with hemodialysis, corticosteroid and immunosuppressive medication)

  4. Pregnancy and breastfeeding

  5. Any comorbid infection requiring

  6. High fever (≥ 38.5 ºC)

  7. Significant leukocytosis (> 15 g/dL)

  8. Abdominal pain worsening in the emergency, impeding ambulation and/or eating

  9. Evidence of generalized peritonitis on physical exam

  10. Intolerance to oral intake and/or persistent vomiting

  11. Marked abdominal distension and/or signs of ileus on CT scan

  12. Noncompliance/unreliability for return visits/lack of support system

  13. Failed outpatient treatment not previously included in study within last 30 days

  14. Cognitive, social or psychiatric impairment

  15. For patients aged 65 years or older, a Charlson Comorbidity Score ≥ 5 as calculated on the following website: https://www.thecalculator.co/health/Charlson-Comorbidity-Index-(CCI)-Calculator-765.ht ml 19-20.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jewish General Hospital Montreal Quebec Canada H3T 1E2

Sponsors and Collaborators

  • Jewish General Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Marylise Boutros, Colorectal Surgery Attending Staff, Assistant Professor of Surgery at McGill University, Jewish General Hospital
ClinicalTrials.gov Identifier:
NCT03146091
Other Study ID Numbers:
  • CODIM-MBM-17-020
First Posted:
May 9, 2017
Last Update Posted:
Aug 18, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Dr. Marylise Boutros, Colorectal Surgery Attending Staff, Assistant Professor of Surgery at McGill University, Jewish General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 18, 2022