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Completed

NCT Number: NCT03794765

Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis

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

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Key information

Age range

13 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Postgraduate Institute of Medical Education and Research

Chandigarh, 160012, India

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Ceftriaxone

Drug

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.

Metronidazole

Drug

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

placebo infusion

Other

Similar placebo infusion

Primary outcomes

  1. Clinical response as defined by the Oxford's criteria

    Time frame: 48 hours

    Patients will be defined as complete responders, partial responders or non-responders

Secondary outcomes

  1. Proportion needing second line therapy

    Time frame: 28 days

    Second line therapy : Intravenous Infliximab, Intravenous cyclosporine or others

  2. Proportion needing colectomy

    Time frame: 28 days

    Number of patients in each group needing colectomy

  3. Mortality

    Time frame: 28 days

    Number of patients in having mortality

  4. Duration of hospital stay

    Time frame: 28 days

    Length of hospital stay in each group

  5. Change in serum CRP levels

    Time frame: 48 hours

  6. Change in Mayo disease severity index

    Time frame: 48 hours

  7. Patients with Reduction in fecal calprotectin by >100 mcg/mg

    Time frame: 48 hours

    Number of patients in each group having the predefined decline in fecal calprotectin

Sponsors and collaborators

Lead sponsor

Post Graduate Institute of Medical Education and Research, Chandigarh

Other

Registry information

Official study title

Use of Antibiotics as an Adjuvant in Patients With Acute Severe Ulcerative Colitis: A Randomised Trial

Acronym: AAASUC

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jan 7, 2019
Registry last updated
Dec 11, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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