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Trial · NCT00333359

Results by group270

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in the International Restless Legs Syndrome Rating Scale (IRLS) at Week 52 Using Observed Case (OC)Naïve; 1200 mg GEn-16.3Standard Deviation 8.23points on a scale
Change From Baseline in the International Restless Legs Syndrome Rating Scale (IRLS) at Week 52 Using Observed Case (OC)Non-naïve; 1200 mg GEn-17.0Standard Deviation 8.20points on a scale
Change From Baseline in the International Restless Legs Syndrome Rating Scale (IRLS) at Week 52 Using Observed Case (OC)All Participants; 1200 mg GEn-16.8Standard Deviation 8.21points on a scale
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 0, n=197, 376, 57384participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 0, n=197, 376, 573300participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCAll Participants; 1200 mg GEnWeek 0, n=197, 376, 573384participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 1, n=185, 363, 548152participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 1, n=185, 363, 548294participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCAll Participants; 1200 mg GEnWeek 1, n=185, 363, 548446participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 4, n=171, 354, 525143participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 4, n=171, 354, 525308participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCAll Participants; 1200 mg GEnWeek 4, n=171, 354, 525451participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 12, n=150, 324, 474133participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 12, n=150, 324, 474297participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCAll Participants; 1200 mg GEnWeek 12, n=150, 324, 474430participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 24, n=138, 305, 443126participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 24, n=138, 305, 443275participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCAll Participants; 1200 mg GEnWeek 24, n=138, 305, 443401participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNaïve; 1200 mg GEnWeek 36, n=132, 281, 413120participants
Number of Participants Classified as Responders to Treatment on the Investigator-rated Clinical Global Impressions of Improvement (CGI-I) at Each Visit Using OCNon-naïve; 1200 mg GEnWeek 36, n=132, 281, 413260participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

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.

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