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

Completed · Phase 2 · Has a placebo group

Conditions studied: Crohn's Disease

In brief

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-mercaptopurine). 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.

Key facts

Study ID

NCT00609973

Run by

University of North Carolina, Chapel Hill

People needed

33

Starts

2008-05-01

Expected to finish

2011-12-01

Last updated by the study team

2013-05-03

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 14 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.

You may not qualify if…

• Short bowel syndrome.
• Previous long term therapy with ciprofloxacin (> 6 weeks prior before surgery)
• 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.
• Dementia
• Uncontrolled Diabetes Type I type II
• Known drug abuse
• Known parasitic disease of the digestive system
• Active replicating Hepatitis B or Hepatitis C
• HIV-infection
• 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.
• Known intolerance/hypersensitivity to ciprofloxacin or other quinolones 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.

Where it is running

• University of North Carolina — Chapel Hill, North Carolina, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.