BAY 0 9867 Cipro Pediatric Use Study (QUIP)

ClinicalTrials.gov ID: NCT00761462

Public ClinicalTrials.gov record NCT00761462. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Nov 7, 2026, 8:09 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Open-label, Non-randomized, Naturalistic, Long-term Safety Surveillance, Observational Study of Either Ciprofloxacin (Either as Oral Suspension, Oral Tablets or Sequential IV Followed by Oral Therapy or Purely IV Therapy) or a Non-quinolone Antibiotic (Either as Oral Suspension, Oral Tablets or Sequential IV Followed by Oral Therapy or Purely IV Therapy) in the Treatment of Pediatric Patients With Infectious Diagnoses

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Objective and subjective musculoskeletal evaluations will be performed to determine differences in the ciprofloxacin versus non-quinolone treated pediatric patients so that we can tell what the natural occurrence of such musculoskeletal conditions is in the general pediatric population.

Study identification

NCT ID: NCT00761462
Recruitment status: Completed
Study type: Interventional
Phase: Phase 3
Lead sponsor: Bayer; Industry
Enrollment: 1,029 participants

Conditions and interventions

Conditions

Infectious Diseases

Interventions

Ciprofloxacin Drug
Non-quinolone antibiotic Drug

Drug

Eligibility (public fields only)

Age range: 2 Months to 16 Years
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Oct 1999 (Type not available)
Primary completion: Jan 2008 (Actual)
Completion: Jan 2008 (Actual)
Last update posted: Jul 31, 2015

1999 – 2008

United States locations

U.S. sites: 66
U.S. states: 29
U.S. cities: 61

Facility	City	State	ZIP	Site status
Not listed	Mobile	Alabama	36608	—
Not listed	Fort Smith	Arkansas	72903	—
Not listed	Corona	California	92879	—
Not listed	Fountain Valley	California	92708	—
Not listed	Long Beach	California	90806	—
Not listed	Orange	California	92868-3974	—
Not listed	Pico Rivera	California	90660	—
Not listed	San Bernardino	California	92411	—
Not listed	San Luis Obispo	California	93405	—
Not listed	Centennial	Colorado	80112	—
Not listed	Denver	Colorado	80218	—
Not listed	Fort Walton Beach	Florida	32548	—
Not listed	Gainesville	Florida	32610-0254	—
Not listed	Hialeah	Florida	33013	—
Not listed	Jacksonville	Florida	32209	—
Not listed	Jupiter	Florida	33458	—
Not listed	Miami	Florida	33155	—
Not listed	Pensacola	Florida	32504	—
Not listed	Tampa	Florida	33606	—
Not listed	Tampa	Florida	33607	—
Not listed	Snellville	Georgia	30078	—
Not listed	Honolulu	Hawaii	96813	—
Not listed	Idaho Falls	Idaho	83404	—
Not listed	Park Ridge	Illinois	60068-1174	—
Not listed	Springfield	Illinois	62701	—
Not listed	Indianapolis	Indiana	46202	—
Not listed	Overland Park	Kansas	66215	—
Not listed	Bardstown	Kentucky	40004	—
Not listed	New Orleans	Louisiana	70118-5799	—
Not listed	Boston	Massachusetts	02115	—
Not listed	Red Wing	Minnesota	55066-0095	—
Not listed	Omaha	Nebraska	68114	—
Not listed	Omaha	Nebraska	68131	—
Not listed	Las Vegas	Nevada	89109	—
Not listed	Hackensack	New Jersey	07601-1991	—
Not listed	Voorhees Township	New Jersey	08043	—
Not listed	New Hyde Park	New York	11040	—
Not listed	New York	New York	10021-4885	—
Not listed	New York	New York	10032	—
Not listed	Stony Brook	New York	11794-8111	—
Not listed	The Bronx	New York	10461	—
Not listed	Durham	North Carolina	27710	—
Not listed	Wilmington	North Carolina	28401	—
Not listed	Akron	Ohio	44308-1062	—
Not listed	Cleveland	Ohio	44109-1998	—
Not listed	Dayton	Ohio	45404-1815	—
Not listed	Youngstown	Ohio	44501-0240	—
Not listed	Oklahoma City	Oklahoma	73104	—
Not listed	Oklahoma City	Oklahoma	73120	—
Not listed	Tulsa	Oklahoma	74135	—
Not listed	Elverson	Pennsylvania	19520	—
Not listed	Havertown	Pennsylvania	19083	—
Not listed	Charleston	South Carolina	29425	—
Not listed	Memphis	Tennessee	38105-2729	—
Not listed	Austin	Texas	78756	—
Not listed	Benbrook	Texas	76126	—
Not listed	El Paso	Texas	79925	—
Not listed	Fort Worth	Texas	76104	—
Not listed	Galveston	Texas	77555-0371	—
Not listed	Houston	Texas	77024	—
Not listed	Houston	Texas	77030	—
Not listed	Temple	Texas	76508	—
Not listed	Layton	Utah	84041	—
Not listed	Norfolk	Virginia	23510	—
Not listed	Richmond	Virginia	23298	—
Not listed	Morgantown	West Virginia	26506	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00761462, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jul 31, 2015 · Synced Nov 7, 2026

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00761462 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →