Trial · NCT07890181
Geographic Mismatch as A Predictor of Short-Term Major Adverse Cardiovascular Events Following Long Coronary Stent Implantation
NCT07890181, Recruiting, Sohag University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Geographic Mismatch as A Predictor of Short-Term Major Adverse Cardiovascular Events Following Long Coronary Stent Implantation. Trials, record NCT07890181. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07890181
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Geographic Mismatch as A Predictor of Short-Term Major Adverse Cardiovascular Events Following Long Coronary Stent Implantation
- NCT number
- NCT07890181
- Status
- Recruiting
- Enrollment
- 650 participants, estimated
- Lead sponsor
- Sohag University
- Conditions
- Geographic Mismatch, Short-Term, Major Adverse Cardiovascular Events, Long Coronary Stent Implantation
- Interventions
- Coronary Stent Implantation
- First posted
- 2026-10-22
- Last updated
- 2026-10-22
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of Major Adverse Cardiovascular Events | 30 days post-percutaneous coronary intervention | Incidence of Major Adverse Cardiovascular Events (MACE) will be recorded within 30 days post-percutaneous coronary intervention (PCI). |
| Secondary | Incidence of all-cause mortality | 60 days post-percutaneous coronary intervention | Incidence of all-cause mortality will be recorded within 60 days. |
| Secondary | Occurrence of myocardial infarction | 30 days post-percutaneous coronary intervention | Number of participants who experience myocardial infarction following the index percutaneous coronary intervention (PCI). |
| Secondary | Occurrence of target lesion revascularization | 30 days post-percutaneous coronary intervention | umber of participants who undergo repeat revascularization of the target lesion following the index percutaneous coronary intervention (PCI). |
| Secondary | Occurrence of definite stent thrombosis | 30 days post-percutaneous coronary intervention | Number of participants who experience definite or probable thrombosis of the stent implanted during the index percutaneous coronary intervention (PCI). |
| Secondary | Hospital readmission | 30 days post-percutaneous coronary intervention | Number of participants who are readmitted to a hospital following discharge from the index percutaneous coronary intervention (PCI) hospitalization. |
| Secondary | Length of index hospital stay | 60 days post-percutaneous coronary intervention | Duration of the index hospitalization during which percutaneous coronary intervention (PCI) is performed, measured in days. |
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.
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/NCT07890181
GET https://conductscience.org/api/trials/v1/NCT07890181/registered