Trial · NCT03446612
Results by group500
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 500
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Daprodustat | ACH 7.5 ug/min, n=2, 2 | 1.1304 | Standard Deviation 0.30030 | Ratio |
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Darbepoetin Alfa | ACH 7.5 ug/min, n=2, 2 | 0.4351 | Standard Deviation 0.17032 | Ratio |
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Daprodustat | ACH 15 ug/min, n=1, 2 | 0.7866 | Standard Deviation NA | Ratio |
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Darbepoetin Alfa | ACH 15 ug/min, n=1, 2 | 0.6183 | Standard Deviation 0.00435 | Ratio |
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Daprodustat | ACH 30 ug/min, n=1, 2 | 1.1328 | Standard Deviation NA | Ratio |
| Change in FBF Ratio in Response to Acetylcholine (Day 1 to Day 42) | Darbepoetin Alfa | ACH 30 ug/min, n=1, 2 | 0.8090 | Standard Deviation 0.28395 | Ratio |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Daprodustat | 7.5 ug/min, n=2, 2 | 8.3180 | Standard Deviation 4.50592 | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Darbepoetin Alfa | 7.5 ug/min, n=2, 2 | -6.0360 | Standard Deviation 3.09976 | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Daprodustat | 15 ug/min, n=1, 2 | -4.6374 | Standard Deviation NA | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Darbepoetin Alfa | 15 ug/min, n=1, 2 | -8.8299 | Standard Deviation 9.98143 | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Daprodustat | 30 ug/min, n=1, 2 | -2.6735 | Standard Deviation NA | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Acetylcholine | Darbepoetin Alfa | 30 ug/min, n=1, 2 | -4.5121 | Standard Deviation 5.66731 | ug/min |
| Change in FBF Ratio in Response to Sodium Nitroprusside (Day 1 to Day 42) | Daprodustat | 3 ug/min | 1.0388 | Standard Deviation NA | Ratio |
| Change in FBF Ratio in Response to Sodium Nitroprusside (Day 1 to Day 42) | Darbepoetin Alfa | 3 ug/min | 0.7420 | Standard Deviation 0.07407 | Ratio |
| Change in FBF Ratio in Response to Sodium Nitroprusside (Day 1 to Day 42) | Daprodustat | 10 ug/min | 2.1447 | Standard Deviation NA | Ratio |
| Change in FBF Ratio in Response to Sodium Nitroprusside (Day 1 to Day 42) | Darbepoetin Alfa | 10 ug/min | 0.7022 | Standard Deviation 0.00860 | Ratio |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Sodium Nitroprusside | Daprodustat | 3 ug/min | -0.2560 | Standard Deviation NA | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Sodium Nitroprusside | Darbepoetin Alfa | 3 ug/min | 0.3844 | Standard Deviation 0.52197 | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Sodium Nitroprusside | Daprodustat | 10 ug/min | 6.8103 | Standard Deviation NA | ug/min |
| Change in the Absolute FBF From Day 1 to Day 42 in Response to Sodium Nitroprusside | Darbepoetin Alfa | 10 ug/min | -0.2873 | Standard Deviation 1.11519 | ug/min |
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
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GET https://conductscience.org/api/trials/v1/NCT03446612/results