check_circleStudy Completed

Acute Exacerbation Of Chronic Bronchitis, Community Acquired Pneumonia, Pelvic Inflammatory

Concentrations of moxifloxacin in gynecological tissues after single i.v. infusion of 400 mg in patients undergoing elective gynecological surgery

Trial purpose

Please see attached Study Results Summary below

Key Participants Requirements

Sex

N/A

Age

28 - 60 Years
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Trial summary

Enrollment Goal
43
Trial Dates
July 2004 - May 2005
Phase
Phase 1
Could I Receive a placebo
N/A
Products
Avelox (Moxifloxacin hydrochloride, BAY12-8039)
Accepts Healthy Volunteer
N/A

Where to participate

StatusInstitutionLocation
Completed
Klinikum der Eberhard-Karls-Universität TübingenTübingen, 72076, Germany
Completed
CRS Clinical-Research-Services Kiel GmbHKiel, 24105, Germany
Terminated
Klinikum der Eberhard-Karls-Universität TübingenTübingen, 72076, Germany

Trial design

Concentrations of moxifloxacin in gynecological tissues after single intravenous infusion of 400 mg in patients undergoing elective gynecological surgery (single-dose, randomized, open-label, prospective, single-center study).
Trial Type
Interventional
Intervention Type
N/A
Trial Purpose
N/A
Allocation
N/A
Blinding
N/A
Assignment
N/A
Trial Arms
N/A