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Trial · NCT00199238

Efficacy of Rupatadine 5, 10 and 20 mg in Chronic Idiopathic Urticaria

NCT00199238, Phase 2, Terminated, J. Uriach and Company

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Efficacy of Rupatadine 5, 10 and 20 mg in Chronic Idiopathic Urticaria. Trials, record NCT00199238. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00199238

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Trial

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

Title
Efficacy of Rupatadine 5, 10 and 20 mg in Chronic Idiopathic Urticaria
NCT number
NCT00199238
Status
Terminated
Phases
Phase 2
Enrollment
248 participants, actual
Lead sponsor
J. Uriach and Company
Conditions
URTICARIA
Interventions
Rupatadine Fumarate
First posted
2005-09-20
Last updated
2022-02-18

Source ClinicalTrials.gov

Registered outcomes4

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

ListOutcomeTime frameDescription
PrimaryPruritus4 weekschange in mean pruritus score (MPS) over the 4-week treatment period.
SecondaryWheals4 weekschange in mean number of wheals score (MNW) over the 4-week treatment period.
Secondarychange in mean total symptoms score (MTSS) over the 4-week treatment period.4 weeks
Secondaryoverall impression4 weeksoverall impression for efficacy was done by the investigator and by the patient

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
17478385RESULT

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/NCT00199238

GET https://conductscience.org/api/trials/v1/NCT00199238/registered