Trial · NCT04776850
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 15 of 15
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Event-free survival (EFS) | At 2 years post-hematopoietic cell transplantation (HCT) | EFS is defined as survival time following HCT without a qualifying event. Will be summarized by the Kaplan-Meier method with 95% confidence intervals. |
| Secondary | Event-free survival | Up to 100 days post-HCT | EFS is defined as survival time following HCT without a qualifying event. Will be summarized by the Kaplan-Meier method with 95% confidence intervals. |
| Secondary | Event-free survival | Up to 1 year post-HCT | EFS is defined as survival time following HCT without a qualifying event. Will be summarized by the Kaplan-Meier method with 95% confidence intervals. |
| Secondary | Overall survival | Up to 100 days post-HCT | Will be summarized by the Kaplan-Meier method. |
| Secondary | Overall survival | Up to 1 year post-HCT | Will be summarized by the Kaplan-Meier method. |
| Secondary | Transplant-related mortality | Up to 30 days post-HCT | Will be summarized by the Kaplan-Meier method. |
| Secondary | Time to platelet and neutrophil engraftment | Up to 2 years post-HCT | Will be estimated using the method of Gooley et al. |
| Secondary | Incidence of graft failure (primary and secondary) | Up to 100 days post-HCT | Will be estimated using the method of Gooley et al. |
| Secondary | Incidence of acute graft-versus-host disease | Up to 100 days post-HCT | Will be estimated using the method of Gooley et al. |
| Secondary | Incidence of chronic graft-versus-host disease | Up to 1 year post-HCT | Will be estimated using the method of Gooley et al. |
| Secondary | Incidence of chronic graft-versus-host disease | Up to 2 years post-HCT | Will be estimated using the method of Gooley et al. |
| Secondary | Incidence of grade II or greater organ toxicity | Up to 100 days post-HCT | Will be reported as counts with percentages. |
| Secondary | Incidence of hepatic sinusoidal obstruction syndrome | Up to 100 days post-HCT | Will be reported as counts with percentages. |
| Secondary | Incidence of central nervous system toxicities including posterior reversible encephalopathy syndrome | Up to 100 days post-HCT | Will be reported as counts with percentages. |
| Secondary | Incidence of infectious complications | Up to 100 days post-HCT | Will be reported as counts with percentages. |
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/NCT04776850/registered