Trial · NCT01542801
Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention
NCT01542801, Phase 4, Completed, Korea University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention. Trials, record NCT01542801. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01542801
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Norfloxacin Versus Ciprofloxacin for Spontaneous Bacterial Peritonitis (SBP) Prevention
- NCT number
- NCT01542801
- Status
- Completed
- Phases
- Phase 4
- Enrollment
- 124 participants, actual
- Lead sponsor
- Korea University
- Conditions
- Adverse Reaction to Other Drugs and Medicines
- Interventions
- Norfloxacin, ciprofloxacin
- First posted
- 2012-03-02
- Last updated
- 2016-12-28
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | The prevention rate of spontaneous bacterial peritonitis (SBP) | 12 months | The incidence of SBP will measured in each the group. Thereby, prevention rate will also be compared between the groups. |
| Secondary | 1 year mortality | 12 months ( 1 year) | liver related mortality and overall mortality will be assessed. |
| Secondary | Incidence of infectious event other than SBP | 12 months | Bacteremia, urinary tract infection, pneumonia, and other infections will be included. |
| Secondary | Hepatorenal syndrome | 12 months | Diagnostic criteria of hepatorenal syndrome is defined by the latest version of Internation ascites club consensus. |
| Secondary | Hepatic encephalopathy | 12 months | Will follow the Western Heaven Criteria. |
| Secondary | Adverse event of drugs | 12 months | Any of adverse event suspected by study drugs will be recorded. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers7
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01542801
GET https://conductscience.org/api/trials/v1/NCT01542801/registered