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NCT01749605 · ClinicalTrials.gov registry record · Phase 4
A Pilot Comparison of Short-course Nitrofurantoin in Females With Uncomplicated Bacterial Cystitis in the Emergency Department
A Phase 4 study, sponsored by University of Iowa.
- Completed
- Registry status
- Phase 4
- Development phase
- 35
- Enrollment target
NCT01749605: Completed Phase 4 study, sponsored by University of Iowa.
NCT01749605 is a Phase 4 study that has completed, run by University of Iowa. The registered enrollment target is 35 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01749605, a Phase 4 study, has completed, sponsored by University of Iowa.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 35 participants
- Enrollment target
Study Summary
Pilot study to compare the efficacy and safety of 3-day, twice-daily regimens of nitrofurantoin and ciprofloxacin in emergency department (ED) patients presenting with UBC.
Primary Outcome
Seven days after randomization, subjects received a telephone call to determine if their symptoms have completely resolved. Patients answers were limited to: Yes (clinical cure), No (treatment failure)
Interventions
- DRUG Nitrofurantoin monohydrate/macrocrystals 100 mg BID x 3 days
- DRUG ciprofloxacin 250 mg BID x 3 days
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 35 participants |
| Start Date | 2010-10 |
| Est. Completion | 2012-01 |
| Phase | Phase 4 |
What the finished NCT01749605 record still lists
NCT01749605 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 35 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (93% lower).
The record links to 0 conditions, and to 2 interventions - of which Nitrofurantoin monohydrate/macrocrystals 100 mg BID x 3 days is the first listed.
NCT01749605 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01749605 about?
NCT01749605 is a clinical study titled "A Pilot Comparison of Short-course Nitrofurantoin in Females With Uncomplicated Bacterial Cystitis in the Emergency Department". Pilot study to compare the efficacy and safety of 3-day, twice-daily regimens of nitrofurantoin and ciprofloxacin in emergency department (ED) patients presenting with UBC.
What is the current status of trial NCT01749605?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 35 participants. The study started on 2010-10. Estimated completion is 2012-01.
What interventions are being tested in trial NCT01749605?
The interventions under investigation include: Nitrofurantoin monohydrate/macrocrystals 100 mg BID x 3 days (DRUG), ciprofloxacin 250 mg BID x 3 days (DRUG).
Who is sponsoring clinical trial NCT01749605?
This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01749605's enrollment target sits among peer trials
35 1506th of 2000 higher than 481 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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