Trial · NCT07900035
Myocardial Injury After Transurethral Resection
NCT07900035, Completed, Haseki Training and Research Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Myocardial Injury After Transurethral Resection. Trials, record NCT07900035. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07900035
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Myocardial Injury After Transurethral Resection
- NCT number
- NCT07900035
- Status
- Completed
- Enrollment
- 89 participants, actual
- Lead sponsor
- Haseki Training and Research Hospital
- Conditions
- Myocardial Injury After Noncardiac Surgery (MINS)
- First posted
- 2026-10-28
- Last updated
- 2026-10-28
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Myocardial Injury After Noncardiac Surgery (MINS) | Within 48 hours after surgery | Percentage of participants who meet the predefined high-sensitivity cardiac troponin T (hs-cTnT) criteria for MINS within 48 hours after surgery. MINS is defined as a postoperative hs-cTnT concentration of 20 to \<65 ng/L with an absolute increase of at least 5 ng/L from the preoperative value, or a postoperative hs-cTnT concentration ≥65 ng/L, after exclusion of overt non-ischemic causes of troponin elevation. Unit of Measure: Percentage of participants with MINS Measurement Tool/Parameter: High-sensitivity cardiac troponin T (hs-cTnT) |
| Secondary | Change in High-Sensitivity Cardiac Troponin T Concentration | Preoperative baseline, 1 hour after surgery, and 48 hours after surgery | hs-cTnT concentrations measured preoperatively before anesthesia, 1 hour after surgery, and 48 hours after surgery will be compared to evaluate perioperative changes. Unit of Measure: ng/L Measurement Tool/Parameter: High-sensitivity cardiac troponin T assay |
| Secondary | Peak Postoperative hs-cTnT Concentration | Within 48 hours after surgery | Highest hs-cTnT concentration measured at the predefined postoperative measurement points. Unit of Measure: ng/L Measurement Tool/Parameter: High-sensitivity cardiac troponin T assay |
| Secondary | Association Between Age and MINS | Preoperative assessment through 48 hours after surgery | Description: Association between participant age and occurrence of MINS. Unit of Measure: Years Measurement Tool/Parameter: Chronological age obtained from medical records |
| Secondary | Association Between Body Mass Index and MINS | Preoperative assessment through 48 hours after surgery | Association between body mass index and occurrence of MINS. Body mass index is calculated as body weight in kilograms divided by height in meters squared. Unit of Measure: kg/m² Measurement Tool/Parameter: Body mass index calculated from measured body weight and height |
| Secondary | Association Between ASA Physical Status and MINS | Preoperative assessment through 48 hours after surgery | Association between American Society of Anesthesiologists physical status classification and occurrence of MINS. Unit of Measure: Percentage of participants in each ASA physical status category Measurement Tool/Parameter: ASA Physical Status Classification System |
| Secondary | Association Between Congestive Heart Failure and MINS | Preoperative assessment through 48 hours after surgery | Association between pre-existing congestive heart failure and occurrence of MINS. Unit of Measure: Percentage of participants with congestive heart failure Measurement Tool/Parameter: Medical history and medical record review |
| Secondary | Association Between Hypertension and MINS | Preoperative assessment through 48 hours after surgery | Association between pre-existing hypertension and occurrence of MINS. Unit of Measure: Percentage of participants with hypertension Measurement Tool/Parameter: Medical history and medical record review |
Source ClinicalTrials.gov
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 34601955 | BACKGROUND |
Source PubMed
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/NCT07900035
GET https://conductscience.org/api/trials/v1/NCT07900035/registered