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

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00609973
Enrollment
33
Registered
2008-02-07
Start date
2008-05-31
Completion date
2011-12-31
Last updated
2013-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Crohn's Disease

Keywords

Postoperative recurrence, inflammatory bowel disease

Brief summary

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.

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.

Interventions

DRUGCiprofloxacin

Ciprofloxacin 500 mg oral bid for 6 months

DRUGPlacebo

Placebo bid for 6 months

Sponsors

Crohn's and Colitis Foundation
CollaboratorOTHER
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of North Carolina, Chapel Hill
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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 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.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
Safety and Tolerability of Ciprofloxacin6 MonthsAdverse events (AE) Discontinuation of study drug due to probably study drug related AE

Secondary

MeasureTime frame
Endoscopic Recurrence Under Postoperative Treatment With Study Medication at 6 Months6 months

Countries

United States

Participant flow

Recruitment details

This study was a pilot multicenter, randomized, double-blind, placebo-controlled trial evaluating the safety and efficacy of ciprofloxacin for the prevention of postoperative recurrence in patients with CD. The study was conducted at 6 centers between January 2008 and March 2011. 33 patients were randomized.

Pre-assignment details

There were no significants events pre-assignment

Participants by arm

ArmCount
Cipro
Ciprofloxacin 500 mg bid
17
Placebo
Placebo bid
16
Total33

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyAdverse Event21
Overall StudyLost to Follow-up21
Overall StudyProtocol Violation43
Overall StudyWithdrawal by Subject01

Baseline characteristics

CharacteristicCiproPlaceboTotal
Age, Customized33 Years27 Years30 Years
Region of Enrollment
United States
17 participants16 participants33 participants
Sex: Female, Male
Female
7 Participants8 Participants15 Participants
Sex: Female, Male
Male
10 Participants8 Participants18 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
8 / 174 / 16
serious
Total, serious adverse events
0 / 171 / 16

Outcome results

Primary

Safety and Tolerability of Ciprofloxacin

Adverse events (AE) Discontinuation of study drug due to probably study drug related AE

Time frame: 6 Months

Population: Intention to Treat analysis.Adverse events (AE), which were classified as probably or possibly related to the study drug.

ArmMeasureGroupValue (NUMBER)
CiproSafety and Tolerability of CiprofloxacinAll AE25 Adverse events
CiproSafety and Tolerability of CiprofloxacinAE probably or possibly related to study drug9 Adverse events
CiproSafety and Tolerability of CiprofloxacinParticipant stops study drug due to AE4 Adverse events
PlaceboSafety and Tolerability of CiprofloxacinAll AE11 Adverse events
PlaceboSafety and Tolerability of CiprofloxacinAE probably or possibly related to study drug1 Adverse events
PlaceboSafety and Tolerability of CiprofloxacinParticipant stops study drug due to AE1 Adverse events
Secondary

Endoscopic Recurrence Under Postoperative Treatment With Study Medication at 6 Months

Time frame: 6 months

Population: Endoscopy 6 months, Intention-to-Treat analysis, patients not undergoing endoscopy were assumed to have endoscopic recurrence

ArmMeasureValue (NUMBER)
CiproEndoscopic Recurrence Under Postoperative Treatment With Study Medication at 6 Months11 participants
PlaceboEndoscopic Recurrence Under Postoperative Treatment With Study Medication at 6 Months11 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026