ConductScience.org, home

Trial · NCT01661621

Results by group32

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

OutcomeGroupCategoryValueSpreadUnits
The Global Response Assessment (GRA) After the Treatment DayGroup 1GRA≥189participants
The Global Response Assessment (GRA) After the Treatment DayGroup 2GRA≥1218participants
The Global Response Assessment (GRA) After the Treatment DayGroup 1GRA<127participants
The Global Response Assessment (GRA) After the Treatment DayGroup 2GRA<161participants
The International Prostate Symptom Score (IPSS) Questionnaires After the Treatment DayGroup 1Baseline14.8Standard Deviation 5.40units on a scale
The International Prostate Symptom Score (IPSS) Questionnaires After the Treatment DayGroup 2Baseline18.0Standard Deviation 6.47units on a scale
The International Prostate Symptom Score (IPSS) Questionnaires After the Treatment DayGroup 11 month11.2Standard Deviation 6.81units on a scale
The International Prostate Symptom Score (IPSS) Questionnaires After the Treatment DayGroup 21 month10.8Standard Deviation 6.36units on a scale
The Maximum Flow Rate (Qmax) After the Treatment DayGroup 1Baseline13.1Standard Deviation 8.10mL/s
The Maximum Flow Rate (Qmax) After the Treatment DayGroup 2Baseline11.4Standard Deviation 5.95mL/s
The Maximum Flow Rate (Qmax) After the Treatment DayGroup 11 month13.6Standard Deviation 7.90mL/s
The Maximum Flow Rate (Qmax) After the Treatment DayGroup 21 month13.6Standard Deviation 6.63mL/s
The Voided Volume After the Treatment DayGroup 1Baseline212.5Standard Deviation 168.8mL
The Voided Volume After the Treatment DayGroup 2Baseline244.0Standard Deviation 148.3mL
The Voided Volume After the Treatment DayGroup 11 month231.6Standard Deviation 163.6mL
The Voided Volume After the Treatment DayGroup 21 month268.3Standard Deviation 150.7mL
The Postvoid Residual Volume (PVR) After the Treatment DayGroup 1Baseline50.1Standard Deviation 62.6mL
The Postvoid Residual Volume (PVR) After the Treatment DayGroup 2Baseline53.9Standard Deviation 58.7mL
The Postvoid Residual Volume (PVR) After the Treatment DayGroup 11 month60.4Standard Deviation 60.4mL
The Postvoid Residual Volume (PVR) After the Treatment DayGroup 21 month42.9Standard Deviation 49.3mL

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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01661621/results