Trial · NCT07248202
Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia in Patients With Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass
NCT07248202, Not applicable, Completed, Cairo University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia in Patients With Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass. Trials, record NCT07248202. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07248202
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia in Patients With Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass
- NCT number
- NCT07248202
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 48 participants, actual
- Lead sponsor
- Cairo University
- Conditions
- Coronary Artery Disease (CAD), Left Ventricular (LV) Systolic Dysfunction, Induction Anesthesia, Coronary Bypass Graft Surgery, Ketamine, Fentanyl, Lidocaine
- Interventions
- Fentanyl (IV), lidocaine
- First posted
- 2025-11-25
- Last updated
- 2026-08-07
Source ClinicalTrials.gov
Registered outcomes13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | average postinduction NIRS | every 5 min after induction of anesthesia until 20 min after | average values of NIRS reading after induction of anesthesia |
| Secondary | mean arterial pressure | every minute after induction of anesthesia until 20 min after induction | invasive mean arterial pressure |
| Secondary | heart rate | every minute after induction of anesthesia until 20 min after induction | bpm |
| Secondary | NRIS | during induction, 1 min after induction, during intubation, then every 5 minutes for 20 min | average of left and right side reading |
| Secondary | cerebral hypoperfusion | during induction, 1 min after induction, during intubation, then every 5 minutes for 20 min | NIRS\<60% or \<90% of baseline reading |
| Secondary | hypotension | immediately after induction of anesthesia until 20 min after induction | mean arterial pressure \<70% of baseline or \<65 mmHg |
| Secondary | extra fentanyl bolus | immediately after induction of anesthesia until 20 min after induction | mcg |
| Secondary | postoperative myocardial infarction | after extubation until 30 days postoperative | elevated troponin and new ECG changes |
| Secondary | postoperative stroke | after extubation until 30 days postoperative | new neurologic deficit |
| Secondary | postoperative acute kidney injury | after extubation until 30 days postoperative |
1 to 10 of 13Source ClinicalTrials.gov
See all 13 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/NCT07248202
GET https://conductscience.org/api/trials/v1/NCT07248202/registered