Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis (AAASUC)
Primary Purpose
Ulcerative Colitis, Inflammatory Bowel Diseases, Acute Severe Colitis
Status
Completed
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
Ceftriaxone
Metronidazole
Placebo infusion
Sponsored by
About this trial
This is an interventional treatment trial for Ulcerative Colitis focused on measuring Antibiotics, Ceftriaxone, Metronidazole
Eligibility Criteria
Inclusion Criteria:
- Acute severe ulcerative colitis as described in European Crohn's and Colitis Organisation (ECCO) guidelines (adapted from Truelove and Witts)
Exclusion Criteria:
- Patients who deny consent
- Age<=12 years
- Pregnant or lactating women
- Severe uncontrolled comorbidities like diabetes mellitus, hypertension, coronary artery disease, chronic liver disease, chronic kidney disease, etc
- History of antibiotic use in the past one month, excluding those who may have received a single dose of antibiotic in past 24 hrs
- History of hypersensitivity or contraindication to steroids or the test drugs
- Presence of toxic megacolon as defined by transverse colon diameter more than 5.5cm on abdominal X-ray
- Patients with evidence of sepsis or active infection
Sites / Locations
- Postgraduate Institute of Medical Education and Research
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Antibiotic
Placebo
Arm Description
Standard of Care (steroids, prophylactic anticoagulation, oral nutrition) And Antibiotics (Inj Ceftriaxone 1 gram intravenous twice daily And Inj Metronidazole 500 mg intravenous thrice daily) for initial 48 hours
Standard of care (steroids, prophylactic anticoagulation, oral nutrition) And Placebo infusions similar to the active drugs
Outcomes
Primary Outcome Measures
Clinical response as defined by the Oxford's criteria
Patients will be defined as complete responders, partial responders or non-responders
Secondary Outcome Measures
Proportion needing second line therapy
Second line therapy : Intravenous Infliximab, Intravenous cyclosporine or others
Proportion needing colectomy
Number of patients in each group needing colectomy
Mortality
Number of patients in having mortality
Duration of hospital stay
Length of hospital stay in each group
Change in serum CRP levels
Change in Mayo disease severity index
Patients with Reduction in fecal calprotectin by >100 mcg/mg
Number of patients in each group having the predefined decline in fecal calprotectin
Full Information
NCT ID
NCT03794765
First Posted
January 4, 2019
Last Updated
December 9, 2020
Sponsor
Postgraduate Institute of Medical Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT03794765
Brief Title
Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis
Acronym
AAASUC
Official Title
Use of Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis: A Randomised Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2019 (Actual)
Primary Completion Date
March 4, 2020 (Actual)
Study Completion Date
April 4, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
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 study is planned as a randomised control trial to study the adjuvant use of antibiotics (ceftriaxone and metronidazole) to achieve a clinical response in hospitalised patients with acute severe ulcerative colitis
Detailed Description
All patients with active ulcerative colitis who present to the Outpatient department or the emergency services of PGIMER shall be screened. Those patients who have acute severe ulcerative colitis shall be assessed for inclusion into the study. Patients who fulfil the eligibility criteria will be randomised into two groups.
Group A will include patients in the intervention arm. They will be given intravenous antibiotics for three days. Injection ceftriaxone 1 gm will be prepared by reconstitution of the crystallized powder form in 100 ml of normal saline. This preparation will then be infused slowly over thirty minutes, after intradermal testing for hypersensitivity. Inj ceftriaxone 1gm IV will be given twelve hourly. Injection metronidazole 500 mg is available from pharmacies in solutions of 100 ml. It will be infused slowly over thirty minutes, three times per day, after intradermal testing for hypersensitivity. Both the drugs will be given for five days. In addition, they will receive the standard of care mentioned below.
Group B will include patients from the placebo arm. They will be given the standard of care as mentioned below. In addition, they will be infused 0.9 % saline of similar quantity, colour, and from similarly shaped bottles, for three days after sensitivity testing with the saline.
Detailed history and examination shall be done for all the patients. History regarding the stool output, any systemic symptoms, prior treatment history and history regarding any precipitant for the acute episode shall be taken. Examination will include vitals (pulse rate, blood pressure, temperature), general physical examination as well as an abdominal examination. All patients will undergo blood investigations on all three days. This includes a complete blood counts, kidney function tests, serum electrolytes, albumin, C-reactive protein, osteopontin, blood culture. Stool routine microscopic examination, fecal calprotectin, stool assay for clostridium difficile toxin will be done. X ray abdomen will be done on all three days to monitor the diameter of transverse colon. Patients will undergo an unprepared sigmoidoscopy with minimal air insufflation and mucosal biopsy. Biopsies will be taken for histological examination. Procalcitonin, fecal calprotectin and CRP shall be repeated on day 3 of admission.
All patients will be prescribed the standard treatment for acute severe colitis, which includes intravenous steroids (Inj Hydrocortisone 100 mg IV QID or Inj Methyprednisolone 60 mg iv OD), anticoagulation, (Inj Unfractionated heparin 5000 IU S/C BD), intravenous fluid supplementation and correction of electrolytes. Patients will be allowed orally and will be prescribed a diet of 25-30 kcal /kg/day.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis, Inflammatory Bowel Diseases, Acute Severe Colitis
Keywords
Antibiotics, Ceftriaxone, Metronidazole
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Antibiotic
Arm Type
Experimental
Arm Description
Standard of Care (steroids, prophylactic anticoagulation, oral nutrition) And Antibiotics (Inj Ceftriaxone 1 gram intravenous twice daily And Inj Metronidazole 500 mg intravenous thrice daily) for initial 48 hours
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Standard of care (steroids, prophylactic anticoagulation, oral nutrition) And Placebo infusions similar to the active drugs
Intervention Type
Drug
Intervention Name(s)
Ceftriaxone
Intervention Description
Injection ceftriaxone 1 gm will be prepared by reconstitution of the crystallised powder form in 100 ml of normal saline. This preparation will then be infused slowly over thirty minutes, after intradermal testing for hypersensitivity. Inj ceftriaxone 1gm IV will be given twelve hourly.
Intervention Type
Drug
Intervention Name(s)
Metronidazole
Intervention Description
Injection metronidazole 500 mg is available from pharmacies in solutions of 100 ml. It will be infused slowly over thirty minutes, three times per day
Intervention Type
Other
Intervention Name(s)
Placebo infusion
Intervention Description
Similar placebo infusion
Primary Outcome Measure Information:
Title
Clinical response as defined by the Oxford's criteria
Description
Patients will be defined as complete responders, partial responders or non-responders
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Proportion needing second line therapy
Description
Second line therapy : Intravenous Infliximab, Intravenous cyclosporine or others
Time Frame
28 days
Title
Proportion needing colectomy
Description
Number of patients in each group needing colectomy
Time Frame
28 days
Title
Mortality
Description
Number of patients in having mortality
Time Frame
28 days
Title
Duration of hospital stay
Description
Length of hospital stay in each group
Time Frame
28 days
Title
Change in serum CRP levels
Time Frame
48 hours
Title
Change in Mayo disease severity index
Time Frame
48 hours
Title
Patients with Reduction in fecal calprotectin by >100 mcg/mg
Description
Number of patients in each group having the predefined decline in fecal calprotectin
Time Frame
48 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Acute severe ulcerative colitis as described in European Crohn's and Colitis Organisation (ECCO) guidelines (adapted from Truelove and Witts)
Exclusion Criteria:
Patients who deny consent
Age<=12 years
Pregnant or lactating women
Severe uncontrolled comorbidities like diabetes mellitus, hypertension, coronary artery disease, chronic liver disease, chronic kidney disease, etc
History of antibiotic use in the past one month, excluding those who may have received a single dose of antibiotic in past 24 hrs
History of hypersensitivity or contraindication to steroids or the test drugs
Presence of toxic megacolon as defined by transverse colon diameter more than 5.5cm on abdominal X-ray
Patients with evidence of sepsis or active infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vishal Sharma
Organizational Affiliation
Postgraduate Institute of Medical Education and Research
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shubhra Mishra
Organizational Affiliation
Postgraduate Institute of Medical Education and Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research
City
Chandigarh
ZIP/Postal Code
160012
Country
India
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
33245002
Citation
Mishra S, Mandavdhare HS, Singh H, Choudhury A, Shah J, Ram S, Kalsi D, Samanta J, Prasad KK, Sharma AK, Dutta U, Sharma V. Adjuvant use of combination of antibiotics in acute severe ulcerative colitis: A placebo controlled randomized trial. Expert Rev Anti Infect Ther. 2021 Jul;19(7):949-955. doi: 10.1080/14787210.2021.1856656. Epub 2020 Dec 14.
Results Reference
result
Learn more about this trial
Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis
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