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OpenTrials
Completed

NCT Number: NCT00488306

Study Evaluating the Safety and Efficacy of Tigecycline in Hospitalized Patients With cIAI

In light of tigecycline's activity against these resistant bacteria, tigecycline may represent a viable new therapy for complicated intra-abdominal infections.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Multiple Cities, Taiwan

About this study

To evaluate the efficacy and safety of tigecycline to treat complicated intra-abdominal infections in hospitalized patients. Both the clinical response profile and the microbiological response profile will be assessed. The primary endpoint will be clinical response within the microbiological evaluable population at the test-of-cure assessment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Hospitalized male or female patients greater than or equal to 18 years of age.
  • Patients must be a candidate for or have had a laparotomy, or laparoscopy of an intra-abdominal abscess.
  • Patients with a complicated intra-abdominal infection such as:
  • an intra-abdominal abscess;
  • an intra-abdominal abscess (including liver and spleen) that develops in a post-operative patient after receiving > 48 hours and less than or equal to 5 days of a non-study antibiotic. An intra-abdominal culture must be obtained from the infected site.
  • appendicitis complicated by perforation (grossly visible) and abscess and/or periappendiceal abscess;
  • perforated diverticulitis complicated by abscess formation or fecal contamination;
  • complicated cholecystitis with evidence of perforation or empyema;
  • perforation of the large or small intestine with abscess, or fecal contamination;
  • purulent peritonitis or peritonitis associated with fecal contamination;
  • gastric or duodenal ulcer perforation with symptoms lasting at least 24 hours prior to operation;
  • traumatic bowel perforation with symptoms lasting at least 12 hours prior to operation.

Exclusion criteria

  • Patients with any concomitant condition that, in the opinion of the investigator, would preclude an evaluation of a response or make it unlikely that the contemplated course of therapy or follow-up visits could be completed.
  • Active or treated leukemia or systemic malignancy that required treatment with chemotherapy, immunotherapy, radiation therapy or antineoplastic therapy within the past 3 months, or any metastatic malignancy to the abdomen with life expectancy less than 6 months.
  • Anticipated length of antibiotic therapy less than 5 days.

Treatment and study plan

tigecycline

Drug

Primary outcomes

  1. The primary efficacy endpoint will be clinical response within the clinically evaluable population at the test-of-cure assessment.

Secondary outcomes

  1. microbiological response (eradicated, persistence, superinfection, or indeterminate) at the patient level, microbiological response (eradicated, persistence, or indeterminate) at the pathogen level (overall and resistant pathogens) clinical

Sponsors and collaborators

Lead sponsor

Wyeth is now a wholly owned subsidiary of Pfizer

Industry

Registry information

Official study title

A Multicenter, Open Label Study to Evaluate the Efficacy and Safety of Tigecycline to Treat Complicated Intra-Abdominal Infections (cIAI) in Hospitalized Patients

Important dates

Study start
2006
Study completion
2007
First posted
Jun 20, 2007
Registry last updated
Jul 7, 2009

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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