Trial · NCT07205757
Adding Lidocaine to Custodiol Mixture
NCT07205757, Phase 4, Recruiting, Fayoum University Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Adding Lidocaine to Custodiol Mixture. Trials, record NCT07205757. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07205757
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Adding Lidocaine to Custodiol Mixture
- NCT number
- NCT07205757
- Status
- Recruiting
- Phases
- Phase 4
- Enrollment
- 70 participants, estimated
- Lead sponsor
- Fayoum University Hospital
- Conditions
- CAD, Arrhythmia Ventricular
- Interventions
- Lidocaine Hydrochloride, Custodiol Solution
- First posted
- 2025-10-03
- Last updated
- 2026-09-01
Source ClinicalTrials.gov
Registered outcomes20
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | incidence of ventricular fibrillation (VF) | Perioperative | incidence of VF occurring after Aorta cross-clamp (ACC) removal |
| Secondary | Troponin I (µg/L) | At immediate postoperatively, 12 and 24 hours postoperative | Troponin I to assess myocardial protection between the two cardioplegia solutions used. |
| Secondary | Number of defibrillator shocks | Perioperative | shocks required to terminate ventricular arrhythmia after ACC removal |
| Secondary | Total volume of cardioplegia solution (in ml). | Perioperative | cardioplegia volume given to the patient |
| Secondary | Total cross-clamp time | from cross clamp until removal of aorta cross clamp up to 6 hours | in minutes |
| Secondary | total CPB time | from starting CPB until weaning from bypass is completed up to 6 hours | in minutes |
| Secondary | Number of grafts | at the end of surgery up to 6 hours | anastomosis coronary grafts |
| Secondary | Time taken to cardiac arrest after cardioplegia infusion | from the start of cardioplegia administration until asystole up to one hour | time to asystole |
| Secondary | Left ventricular ejection fraction assessed both preoperative and after 24 hours postoperatively. | assessed both preoperative and after 24 hours postoperatively. | echo assessment |
| Secondary | Preoperative EURO II score | assessed preoperatively at the start of patient enrollment | EURO II score |
1 to 10 of 20Source ClinicalTrials.gov
See all 20 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.
Papers9
The papers the trial lists on ClinicalTrials.gov.
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/NCT07205757
GET https://conductscience.org/api/trials/v1/NCT07205757/registered