Ciprofloxacin for the Prevention of Postoperative Endoscopic Recurrence in Crohn's Disease

Condition(s) targeted: Crohn's Disease

Intervention: Ciprofloxacin (Drug); Placebo (Drug)

Phase: Phase 2

Status: Recruiting

Sponsored by: University of North Carolina

Official(s) and/or principal investigator(s):
Hans H Herfarth, MD, PhD, Principal Investigator, Affiliation: University of North Carolina

Overall contact:
Hans H Herfarth, MD, PhD, Phone: 919 9666806, Email: hherf@med.unc.edu

Despite extensive medical treatment, surgical resection is required in approximately 70% of the patients at some time. However, recurrence of the disease after operation occurs in the majority of patients and is a serious limitation of surgical management. Therapeutic options to maintain postoperative clinical remission are urgently needed. Several drugs including mesalazine, antibiotics (metronidazole, ornidazole) and azathioprine or 6-mercaptopurine have been studied in the past. But the efficacy is very limited (mesalazine), overshadowed by intolerability during long-term therapy (metronidazole, ornidazole) or inconclusive (azathioprine or 6-mercaptopurin). Research demonstrating the absence of inflammation in patients with diverting ileostomy and the clinical benefit of a postoperative antibiotic therapy using metronidazole or ornidazole implicates a role of the resident bacterial flora in the postoperative relapse. Ciprofloxacin has a broad antibacterial spectrum. More interestingly it also suppresses E. coli strains, which can be found in high numbers in early and chronic ileal lesions of Crohn's disease patients Ciprofloxacin has demonstrated beneficial effects in the therapy of inflammatory bowel diseases, but the available data of the effectiveness of ciprofloxacin allow only a very limited judgement of the safety and tolerability of a 6 months therapy of ciprofloxacin. Therefore an exploratory multicenter prospective, placebo-controlled trial is planned to analyze the safety and tolerability of a 6 months therapy with ciprofloxacin compared to placebo in 40 patients (randomly assigned in a 1: 1 ratio) undergoing ileocecal resection (or resection of parts of the colon). If this therapeutic regimen demonstrates tolerability, a second larger study improving the superiority of ciprofloxacin versus placebo can be initiated.

Official title: Double-Blind, Placebo Controlled, Randomized, Multicentre, Pilot Study on the Safety and Efficacy of Ciprofloxacin for Prophylactic Prevention of Postoperative Endoscopic Recurrence in Crohn's Disease Patients

Study design: Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator), Parallel Assignment

Primary outcome: Safety and tolerability of ciprofloxacin

Secondary outcome: Endoscopic recurrence under postoperative treatment with study medication at 6 months

Detailed description: Despite extensive medical treatment, surgical resection is required in approximately 70% of the patients at some time. However, recurrence of the disease after operation occurs in the majority of patients and is a serious limitation of surgical management. In this setting the bacterial flora plays an important role as demonstrated by the benefit of a postoperative antibiotic therapy with either metronidazole or ornidazole or the absence of inflammation in patients with diverting ileostomy. However, both aforementioned antibiotic regimens have numerous adverse events limiting the value of this therapy in daily clinical practice. Ciprofloxacin suppresses the gram negative aerobic bacterial flora including E. coli strains, which can be found in early and chronic ileal lesions of Crohn's disease patients. A limited number of clinical data suggest efficacy of this drug in patients with established Crohn's disease. This exploratory multicenter prospective, placebo-controlled trial will analyze the safety and tolerability of a 6 months therapy with ciprofloxacin compared to placebo in 40 patients (randomly assigned in a 1: 1 ratio) undergoing ileocecal resection (or resection of parts of the colon) with primary anastomosis. No other treatments for Crohn's disease will be permitted. The primary objective of this study is to assess the safety and tolerability of a 6 months therapy of ciprofloxacin (500 mg bid) vs. placebo tablets for prevention of endoscopic recurrence in postoperative Crohn's disease patients. The secondary objectives of this study are to evaluate the endoscopic recurrence in the neoterminal ileum and at the ileocolonic anastomosis as well as the extent of colonic lesions. Additionally bioptic samples at the anastomotic site and patient DNA samples will be collected for later analysis of bacterial ribosomal 19S RNA and DNA polymorphisms (such as NOD2 or IL-23). The clinical data generated by this study will serve as a basis for a definitive clinical trial investigating the effectiveness of ciprofloxacin in the prevention of endoscopic recurrence in postoperative Crohn's disease.

Minimum age: 18 Years. Maximum age: 70 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Signed informed consent.

- Man or woman between 18 and 70 years of age.

- Diagnosis of Crohn's disease confirmed during index surgery.

- Detailed assessment of disease localization by colonoscopy, small bowel radiography,

and/or other appropriate methods (e. g., MRI, CT) within 6 months prior inclusion into the study.

- Resection for ileal or ileo-colonic Crohn's disease with ileo-colonic anastomosis

(i. e., without grossly visible disease at the resection margins); neoterminal ileum should be assessable by endoscopy.

- Ability to start oral nutrition and medication intake within 8 days after index

surgery.

- Negative pregnancy test at screening visit in females of childbearing potential.

- Use of appropriate contraceptive methods for females of childbearing potential and

males with procreative capacity during treatment.

Exclusion Criteria:

- Short bowel syndrome.

- Patients in whom any visible lesions at the anastomosis were left after index

surgery.

- Serious secondary illnesses of an acute or chronic nature, which in the opinion of the

Investigator renders the patient unsuitable for inclusion into the study.

- Seizure disorder.

- Serum creatinine levels exceeding 1. 5 mg/dL or 130 μmol/L.

- Presence of an ileal or colonic stoma.

- Known previous or concurrent malignancy (other than that considered surgically cured,

with no evidence for recurrence for 5 years).

- Application of non-steroidal anti-inflammatory drugs as long term treatment.

- Previous long term therapy with ciprofloxacin.

- Known intolerance/hypersensitivity to ciprofloxacin or other quinolons or drugs of

similar chemical structure or pharmacological profile.

- Chronic use of CYP1A2 substrates (aminophylline, fluvoxamine, mexiletine, mirtazapine,

ropinirole, tizanidine, trifluoperazine).

- Well-founded doubt about the patient's cooperation.

- Existing pregnancy, lactation, or intended pregnancy or impregnation within the next 3

months.

- Non-use of appropriate contraceptives in females of childbearing potential (e. g.

condoms, intrauterine device [IUD], hormonal contraception for females, or a means of contraception for a particular patient considered adequate by the responsible investigator) during treatment.

- Participation in another clinical trial within the last 30 days, simultaneous

participation in another clinical trial, or previous participation in this trial.

Hans H Herfarth, MD, PhD, Phone: 919 9666806, Email: hherf@med.unc.edu

University of North Carolina, Chapel Hill, North Carolina 27599, United States; Recruiting
Dolly Walkup, Phone: 919-843-8105, Email: dolly_walkup@med.unc.edu
Hans H Herfarth, MD, PhD, Principal Investigator

Starting date: January 2008
Ending date: January 2011
Last updated: February 6, 2008