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NCT07847580Not yet recruiting

Intranasal Dexmedetomidine and Perioperative Myocardial Injury in Patients Having Percutaneous Coronary Interventions

Intranasal Dexmedetomidine and Perioperative Myocardial Injury in Patients Having Percutaneous Coronary Interventions: A Prospective, Multi-Center Randomized Trial

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

The goal of this clinical trial is to determine the effect of pre-operative dexmedetomidine on periprocedural myocardial injury in patients having percutaneous coronary intervention (PCI). The specific research hypothesis is that intranasal administration of 100 μg dexmedetomidine (DEX) reduces the incidence of periprocedural myocardial injury within 48 hours after PCI, as compared with normal saline. Participants will be randomly assigned in a 1:1 ratio to two groups: the dexmedetomidine group and the placebo group.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
2500 (estimated)
First submitted
16 Sept 2026
Start date
30 Sept 2026
Primary completion date
30 Jun 2029
Lead sponsor
Second Affiliated Hospital, Zhejiang University, School of Medicine
NCT number
NCT07847580

What you commit to

  • Study type: Interventional
  • Planned participants: 2500
  • From 30 Sept 2026 to the primary completion date, 30 Jun 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of drugs that may interfere with the study medication within 1 week before surgery, including α2-adrenergic receptor agonists (e.g., clonidine) or antagonists, and tricyclic antidepressants;

Other illness

  • Allergy or contraindication to dexmedetomidine, including severe sinus bradycardia (resting heart rate \< 50 beats/min), sick sinus syndrome, second-degree or higher atrioventricular block without pacemaker implantation;
  • Uncontrolled hypertension (systolic blood pressure \> 180 mmHg or diastolic blood pressure \> 110 mmHg) or hypotension (systolic blood pressure \< 90 mmHg);
  • Language, visual, or hearing impairment that may affect questionnaire assessment;

Lab values

  • Patients with severe cardiac insufficiency (left ventricular ejection fraction \< 40% or New York Heart Association functional class Ⅲ-IV), cardiogenic shock, or hemodynamic instability;
  • Hepatic or renal insufficiency (Alanine Aminotransferase/Aspartate Aminotransferase/Creatinine \> 3 times the upper limit of normal);

Other

  • BMI \> 30 kg/m²;
  • Known or suspected sleep apnea;
  • Nasal anatomical abnormalities interfering with nasal spray administration;
  • Pregnant or lactating women;
  • Participation in another clinical trial that may conflict with this trial.

Who the study is looking for

  • Aged 45-85 years(inclusive);
  • Able to confirm understanding of risks, benefits, and treatment alternatives of receiving intranasal dexmedetomidine, and he/she or his/her legally authorized representative provides written informed consent prior to any study-related procedure.
  • Diagnosed with coronary artery disease with objective evidence of ischemia or silent ischemia, meeting the indications for elective PCI.
  • Designated American Society of Anesthesiologists (ASA) physical status II-Ⅲ (ranging from mild systemic disease to severe underlying conditions; patients with marked limitation in ordinary physical activity, yet still capable of light daily activities).

Age in the registry: 45 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Second Affiliated Hospital of Zhejiang University School of Medicine
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.