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Trial · NCT05691764

Effect of Cyclosporine and Remote Ischemic Preconditioning in Reperfusion Ischemia Injury on Tetralogy Fallot Patients With Correction Surgery

NCT05691764, Not applicable, Completed, Universitas Indonesia

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Effect of Cyclosporine and Remote Ischemic Preconditioning in Reperfusion Ischemia Injury on Tetralogy Fallot Patients With Correction Surgery. Trials, record NCT05691764. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05691764

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Effect of Cyclosporine and Remote Ischemic Preconditioning in Reperfusion Ischemia Injury on Tetralogy Fallot Patients With Correction Surgery
NCT number
NCT05691764
Status
Completed
Phases
Not applicable
Enrollment
40 participants, actual
Lead sponsor
Universitas Indonesia
Conditions
Myocardial Injury, Cardiac Surgery
Interventions
Cyclosporin, remote ischemic preconditioning, Placebo
First posted
2023-01-20
Last updated
2023-01-20

Source ClinicalTrials.gov

Registered outcomes7

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryMalondialdehyde (MDA)1 yearROS level is determined by measuring MDA concentration (nmol/mL)
PrimaryCalcium cytosol concentration1 yearCalcium concentration (nmol/mL) in cytosol is determined by ratiometric analysis on Fura Red- dyed heart cells.
PrimaryMitochondrial edema1 yearMitochondrial edema (%) is measured by decreasing of optical density that indicates change in mitochondrial matrix volume.
SecondaryCardiac index1 yearExamined with echocardiography, unit of measurement is litres per minute per square metre (L/min/m2).
SecondaryTroponin I1 yearMeasured from venous blood, unit of measurement is nanograms per milliliter (ng/mL).
SecondaryCreatine kinase- MB (CKMB)1 yearMeasured from venous blood, unit of measurement is units per liter (IU/L).
SecondaryVasoactive inotropic score (VIS)1 year
VIS was calculated as: dopamine dose (μg/kg/min) + dobutamine dose (μg/kg/min) + 100 × epinephrine dose (μg/kg/min) + 10 × milrinone dose (μg/kg/min) + 10 000 × vasopressin dose (unit/kg/min) + 100 × norepinephrine dose (μg/kg/min).

Outcomes0

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.

Papers4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
12411407RESULTPubMed
25720581RESULTPubMed
28329231RESULTPubMed
30621955RESULTPubMed

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT05691764

GET https://conductscience.org/api/trials/v1/NCT05691764/registered