Multiple Cities, Taiwan
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.
Looking for future studies?
Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
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
DrugPrimary outcomes
-
The primary efficacy endpoint will be clinical response within the clinically evaluable population at the test-of-cure assessment.
Secondary outcomes
-
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.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Open to Laparoscopic Reverse Conversion of Perforated Appendicitis
NCT05283733
Abdominal Abscess, Abscess
Zagazig, Egypt
View Trial DetailsUse of Iterative Reconstruction Method in Ultralow-dose CT for Follow-up of Patients With Intraabdominal Abscess: Comparison With Standard Dose CT
NCT03681665
Abdominal Abscess, Abscess
Seoul, South Korea
View Trial DetailsA Safety and Tolerability Study of Doripenem in Patients With Abdominal Infections or Pneumonia
NCT00515034
Abdominal Abscess, Abscess
View Trial DetailsAlteplase for Percutaneous Treatment of Loculated Abdominopelvic Abscesses
NCT00284739
Abdominal Abscess, Abscess
Honolulu, Hawaii, United States
View Trial Details