Trial · NCT07903428
Improving Deceased Organ Donation and Transplantation Using the Donation Advisor Clinical Decision Support Tool
NCT07903428, Not applicable, Not yet recruiting, OBS Medical Ltd
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Improving Deceased Organ Donation and Transplantation Using the Donation Advisor Clinical Decision Support Tool. Trials, record NCT07903428. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903428
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Improving Deceased Organ Donation and Transplantation Using the Donation Advisor Clinical Decision Support Tool
- NCT number
- NCT07903428
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 10 participants, estimated
- Lead sponsor
- OBS Medical Ltd
- Conditions
- Organ Donation After Circulatory Death, Organ Donation, Clinical Decision Support Tool
- Interventions
- Donation Advisor clinical decision-support tool
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Enrolment | 12 months | (i) Average enrolment of 1 patient/centre/2 months |
| Primary | Consent rate | 12 months | (ii) We will target a consent rate of \> 90%. |
| Primary | Protocol adherence | 12 months | (iii) We will target \> 96% protocol adherence defined by successful predictive model and DA report generation, for both the preWLSM and postWLSM reports, with red light upper cutoffs of 70%. |
| Primary | DA report delivery (a) | 12 months | (iv) a) We will target \>96% confirmed delivery of DA report to at least one transplant physician and donation physician to assist clinical decision-making in the intervention arm, for both the preWLSM and postWLSM reports, with red light upper cutoffs of 70%. |
| Primary | DA report delivery (b) | 12 months | (iv) b) We will target \>85% successful generation and delivery (to at least one transplant physician and donation physician) of both reports, with a red-light upper cutoff of 58%. Of the primary outcome measurements, this applies only to the intervention arm. |
| Primary | Outcome Data Collection (a) | 18 months | (a) proportion of patients consented for DCC that proceed to DCC attempt |
| Primary | Outcome Data Collection (b) | 18 months | (b) proportion of successful and unsuccessful DCC attempts |
| Primary | Outcome Data Collection (c) | 18 months | (c) time to death of all patients consented for DCC |
| Primary | Outcome Data Collection (d) | 18 months | (d) organs retrieved |
| Primary | Outcome Data Collection (e) | 18 months | (e) organs transplanted |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 registered outcomesOutcomes0
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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.
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/NCT07903428
GET https://conductscience.org/api/trials/v1/NCT07903428/registered