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Preventing Contrast-induced Nephropathy: Evaluating Hydration Strategies and L-carnitine Administration

NCT01786824 on ClinicalTrials.gov Phase 3 Centre Hospitalier Universitaire de Nīmes (academic or other) Started 2014-12-31 Terminated
Riskier than 49% of active trials
this trial: 16% 0% 36%

Model scores of the 29,894 trials active now.

Model score 16% for any early termination, 10% for termination due to slow enrollment. Past trials like this one (phase, sponsor type and disease area, started 2008–2016) ended terminated 15% of the time (169 trials).

Finished trial that started 2008–2014: scored by a model trained without any trial from its start year, so its own outcome was never used.

How it ended

Terminated on 2015-08-31, after 2014-12-31 start.

Reason given by the sponsor: “other”

The score above never used this outcome: finished trial that started 2008–2014: scored by a model trained without any trial from its start year, so its own outcome was never used.

Termination over time, as the model saw it at the start

0% 17% 34% 51% 68% 0123456 yr completed 59% terminated 32%

Cumulative chance of ending terminated (red) or completed (green) by each year from its start; it actually ended on 2015-08-31. The rest of the way to 100% is still running.

From the competing-risks survival model (termination vs completion, still-running trials censored), fit to trials that started 2008–2014 and recalibrated to termination rates over 2022–2024, since termination has become more common. Checked on past years, it still ran a little low when the rise continued.

What moved the score

Every input that moved this score, largest first: SHAP contributions in log-odds, red raising risk and green lowering it. They describe the model, not causes of termination. Phrases are traced from the text features back to this registration's words, approximately.

The trial

Design

Phase
3 (typical: 2)
Number of arms
4 (typical: 2)
Allocation
randomized
Design
factorial (typical: parallel)
Primary purpose
prevention (typical: treatment)
Blinding
none
Has a data monitoring committee
Yes (typical: 56% yes)
Responsible party
sponsor
Collaborators
0
Keywords listed
3 (typical: 1)

Who can join

Minimum age
18
Maximum age
not given (typical: 71)
Sex
all
Accepts healthy volunteers
No (typical: 9% yes)

Sponsor's track record

Sponsor type
academic or other
Sponsor's past trials
37 (typical: 32)
Sponsor's past termination rate
16.2% (typical: 9.9%)
Trials the sponsor started in the prior 2 years
28 (typical: 19)

Drug's FDA history

Drugs with FDA adverse-event history
2 (typical: 1)
Drug has FAERS history
Yes (typical: 64% yes)
Drug's FAERS reports before start
82682 (typical: 2148)
Drug's FAERS reports in the prior 12 months
15779 (typical: 412.5)
Drug's FAERS reports marked serious
81.0% (typical: 85.6%)
Drug's FAERS reports with a death
11.9% (typical: 15.9%)

Disease area and drugs

Disease areas
urogenital
Drugs matched to FDA substances
bicarbonate, carnitine

Typical values are among the trials active now. Sponsor and drug history are counted only up to this trial's start date.

Similar finished trials

Closest by meaning of the registration text (PubMedBERT embeddings), among finished trials. How they ended is context, not an input to this trial's score.