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NCT07195968Enrolling by invitation

Comparative Analysis of NTG-Pd/Pa and Saline-Pd/Pa (CANS)

A Prospective, Multicenter Study: Comparative Analysis of NTG-Pd/Pa and Saline-Pd/Pa

Source: ClinicalTrials.gov · Last updated 29 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this observational study is to compare the value of NTG-Pd/Pa and saline-Pd/Pa in participants with intermediate stenosis of the coronary artery. The main questions it aims to answer are: The numerical difference between NTG-Pd/Pa and saline-Pd/Pa To compare the diagnostic performance of NTG-Pd/Pa and saline-Pd/Pa in predicting the binary result of FFR assessment? Participants will undergo NTG-Pd/Pa, Saline-Pd/Pa, and FFR successively in the target vessel.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
50 (estimated)
First submitted
18 Sept 2025
Start date
17 Sept 2025
Primary completion date
31 May 2027
Lead sponsor
National Taiwan University Hospital
NCT number
NCT07195968

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 17 Sept 2025 to the primary completion date, 31 May 2027
  • 3 sites 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.

Other illness

  • Resting heart rate is less than 50 beats per minute.
  • Heart failure remains decompensated at the time of examination, such as inability to lie flat or cardiogenic shock.
  • Acute onset of asthma or chronic obstructive pulmonary disease.

Other

  • Systolic blood pressure is less than 90 mmHg for more than 5 minutes during examination.

Who the study is looking for

  • Participants with coronary artery with 50-90% stenosis.
  • In participants who suffered from ST elevation myocardial infarction within 5 days, only the non-culprit vessel was eligible for coronary functional testing.

Age in the registry: 21 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

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

SiteCityCountrySite status
National Taiwan University Hospital Hsin-Chu Hospital
Coordinator of this site? Confirm its status
HsinchuTaiwanUnknown status
Miaoli General Hospital, Ministry of Health and Welfare
Coordinator of this site? Confirm its status
MiaoliTaiwanUnknown status
Taichung Veterans General Hospital
Coordinator of this site? Confirm its status
TaichungTaiwanUnknown status

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