CClinicalTrials.gg
CompletedNCT00769171DRAGONUpdated Dec 18, 2014

Dragon Study (the Safety and Efficacy for Treatment of Patients With Complicated Intra Abdominal Infections)

A Phase 3 interventional study of Avelox (Moxifloxacin, BAY12-8039) and Ceftriaxone + Metronidazole in Infection, Intra-abdominal, sponsored by Bayer. Completed at 25 sites in 6 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-12-18.

Sponsored by Bayer · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
364
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to assess the safety and efficacy of intravenous administration Moxifloxacin (BAY 12-8039) compared to intravenous ceftriaxone and metronidazole for the treatment of patients with complicated intra abdominal infections. In view of the fact that intra abdominal infections are typically polymicrobial and are often treated empirically, the selected antibacterial agent must cover the likely spectrum of bacterial pathogens. Combination antibiotics therapy has been widely used with great success.

02

Conditions studied

  • Infection, Intra-abdominal

Keywords

  • Complicated Intra-Abdominal Infections
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 364 is above the median of 120 across 4,200 interventional studies indexed under Infections.

Browse Infections studies →

Lead sponsor

Bayer is the lead sponsor of 1,643 studies on the registry; 57 are open to participants now.

Of its 209 completed or terminated interventional studies of FDA-regulated products, 129 (62%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Hospitalized males or females >/= 18 years of age
  • Expected duration of treatment with intravenous antibiotics in hospital is anticipated to be >/= 3 full days but not exceeding 14 days
  • Ability to provide written informed consent
  • Confirmed or suspected intra abdominal infection through surgical procedure or Radiological evidence. For suspected intra abdominal infection, The patient must be scheduled for a surgical procedure

Exclusion criteria

Exclusion Criteria:

  • Known hypersensitivity to fluoroquinolones, or other quinolones, and/or to beta lactams antibiotic drugs, or metronidazole or any of the excipients. History of tendon disease/disorder related to quinolone treatment
  • Known congenital or documented acquired QT prolongation; uncorrected hypokalemia; clinically relevant bradycardia; clinically relevant heart failure with reduced left ventricular ejection fraction; previous history of symptomatic arrhythmias. Concomitant use of any of the following drugs, reported to increase the QT interval:
  • Known severe end stage liver disease (Child Pugh C)
  • Systemic antibacterial therapy for more than 24 h within 7 days of enrollment
  • Indwelling peritoneal catheter, Pre existing ascites and presumed spontaneous bacterial peritonitis
  • All pancreatic processes including pancreatic sepsis, peripancreatic sepsis, or an intra abdominal infection secondary to pancreatitis
  • Traumatic perforation of the upper gastrointestinal tract (stomach, duodenum) or perforated peptic ulcer if duration of perforation is \< 24 h or if operated on within 24 h of perforation
  • Traumatic perforation of the small or large bowel if duration of perforation is \< 12 h or if operated on within 12 h of perforation
  • Transmural necrosis of the intestine due to acute embolic, thrombotic, or obstructive occlusions
  • Acute cholecystitis with infection confined to the gallbladder unless there is evidence of an abscess or necrotic tissue or purulent exudate surrounding the gallbladder indicating a transition of bacteria and the inflammatory process into the abdominal cavity
  • Early acute or suppurative, nonperforated appendicitis unless there is evidence of an abscess or peritoneal fluid containing leukocytes and micro organisms suggestive of regional contamination
  • Infections originating from the female genital tract. Perinephric infections
  • Severe, life threatening disease with a life expectancy of \< 48 h or APS and APACHE scores of > 35, Known rapidly fatal underlying disease (death expected within 6 months)
  • Neutropenia (neutrophil count \< 1,000/microliter) caused by immunosuppressive therapy or malignancy
  • Patients known to have AIDS or HIV seropositives who are receiving HAART
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
364 participants (actual)

Study arms

  • Active comparator
    Arm 2

    Drug: Ceftriaxone + Metronidazole

  • Experimental
    Arm 1

    Drug: Avelox (Moxifloxacin, BAY12-8039)

Interventions

  • DrugAvelox (Moxifloxacin, BAY12-8039)

    Moxifloxacin 400 mg every 24 h

  • DrugCeftriaxone + Metronidazole

    Ceftriaxone 2 g every 24 h and Metronidazole 500 mg every 12 h

06

What researchers measure

Primary outcomes

  1. Clinical Response

    Time frame: After 10-14 days of treatment

Secondary outcomes

  1. Clinical and bacteriological response

    Time frame: During 3-5days of treatment

  2. Bacteriological and radiological response

    Time frame: After 10-14 days of treatment

  3. Clinical response at the TOC visit in patients with bacteriological proven intra abdominal infection

    Time frame: After 10-14 days of treatment

  4. Mortality attributable to intra abdominal infection

    Time frame: 13-28 days

07

Study locations

25 sites
  • Nanjing, Jiangsu, China
  • Chengdu, Sichuan 610041, China
  • Hangzhou, Zhejiang 310003, China
  • Beijing, 100044, China
  • Beijing, 100050, China
  • Beijing, 100730, China
  • Beijing, China
  • Shanghai, 200032, China
  • Shanghai, 200127, China
  • Shanghai, 200233, China
  • Shanghai, China
  • Tianjin, 300000, China
  • Shatin, New Territories, Hong Kong
  • Hong Kong, Hong Kong
  • Bandung, West Java 40161, Indonesia
  • Uijeongbu, Kyonggi-do 480-130, Korea, Republic of
  • Incheon, 405-760, Korea, Republic of
  • Seoul, 137-701, Korea, Republic of
  • Seoul, 150-713, Korea, Republic of
  • Seoul, 420-717, Korea, Republic of
  • Kuching, Sarawak 93400, Malaysia
  • Terengganu, 20400, Malaysia
  • Kaoshiung, 813, Taiwan
  • Tainan, 70428, Taiwan
  • Taipei, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00769171
Lead sponsor
Bayer
First posted
Oct 8, 2008
Start date
Oct 2005
Primary completion
Dec 2006
Completion
Jan 2007
Last update
Dec 18, 2014

Study contacts

Bayer Study Director
study director · Bayer

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion