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Trial · NCT00142272

Single Dose Ciprofloxacin in the Treatment of Childhood Cholera:Randomized Controlled Clinical Trial

NCT00142272, Phase 3, Completed, International Centre for Diarrhoeal Disease Research, Bangladesh

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Single Dose Ciprofloxacin in the Treatment of Childhood Cholera:Randomized Controlled Clinical Trial. Trials, record NCT00142272. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00142272

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Single Dose Ciprofloxacin in the Treatment of Childhood Cholera:Randomized Controlled Clinical Trial
NCT number
NCT00142272
Status
Completed
Phases
Phase 3
Enrollment
180 participants
Lead sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Conditions
Cholera
Interventions
Ciprofloxacin
First posted
2005-09-02
Last updated
2022-02-11

Source ClinicalTrials.gov

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryRates of clinical success
SecondaryRates of bacteriologic success at test of cure visit.
SecondaryDuration of diarrhoea.
SecondaryRates of clinical relapse.
SecondaryRates of bacteriologic relapse.
SecondaryDuration of faecal excretion of V. cholerae O1 or V. cholerae O139.
SecondaryMeasurements of six-hourly volume of watery stool will be done for the period in which patients are hospitalised.
SecondaryProportion of patients requiring unscheduled intravenous fluids.
SecondaryFrequency of vomiting and its volume.
SecondaryFrequency of stool per day.

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
16182896DERIVED

Source PubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT00142272

GET https://conductscience.org/api/trials/v1/NCT00142272/registered