CClinicalTrials.gg
Status unknownNCT02284048Updated Nov 6, 2014

Effect of Ticagrelor on Adenosine-Induced Coronary Flow Reserve in Patients With Microvascular Angina

A Phase 4 interventional study of ticagrelor in Microvascular Angina, sponsored by Second Xiangya Hospital of Central South University. Status unknown. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2014-11-06.

Sponsored by Second Xiangya Hospital of Central South University · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
140
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
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Study summary

This study is undertaken to determine if ticagrelor augments adenosine-induced coronary flow reserve (CFR), ameliorates clinical symptomatology and exercise tolerance in patients with MVA

Read the detailed description

Considering the reduced CFR and increased platelet aggregability in patients with MVA, together with the augmented effect on adenosine-mediated coronary blood flow and potent antiplatelet effect of ticagrelor, we speculate that ticagrelor can promisingly ameliorate the coronary microvascular function in patients with MVA.

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Conditions studied

  • Microvascular Angina

Keywords

  • Ticagrelor
  • Coronary Flow Reserve
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In context

Angina Pectoris

519 studies on the registry are indexed under Angina Pectoris; 82 are open to participants now.

This study's planned enrollment of 140 is above the median of 123 across 336 interventional studies indexed under Angina Pectoris.

Browse Angina Pectoris studies →

Lead sponsor

Second Xiangya Hospital of Central South University is the lead sponsor of 82 studies on the registry; 48 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

For inclusion in the study subjects should fulfill the following criteria:

  1. Provision of informed consent prior to any study specific procedures
  2. Female or male aged 18-80 years
  3. A diagnosis of stable primary MVA based on the presence of

    • a history of typical effort angina,
    • exercise-induced ST-segment depression>1 mm,
    • normal or near-normal (coronary artery stenosis\<50%) coronary angiography,
    • absence vasospastic angina
    • a coronary flow reserve (CFR) \<2.5 in the left anterior descending coronary artery as assessed by coronary blood flow (CBF) response to adenosine at transthoracic Doppler echocardiography
    • suboptimal control of symptoms on conventional anti-ischemic therapy, as indicated by the occurrence of >1 episode per week of angina

Exclusion criteria

Exclusion Criteria:

ubjects should not enter the study if any of the following exclusion criteria are fulfilled:

  1. concomitance with any of the cardiac condition below

    • significant (>50%)coronary plaque disease
    • coronary artery spasm at angiography or other evidence of vasospastic angina
    • valvular or other structural heart disease
    • uncontrolled hypertension
    • abnormal echocardiographic examination including left ventricular hypertrophy
  2. no previous consumption of the ticagrelor
  3. no apparent contraindications to ticagrelor administration.

    • History of Intracranial Hemorrhage
    • Active Bleeding
    • Severe Hepatic Impairment: AST and ALT are greater than 3 times of the upper limit. Bilirubin is greater than the upper limit.
    • hypersensitivity (e.g. angioedema) to ticagrelor or any component of the product
    • severe COPD or asthma
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
140 participants (estimated)

Study arms

  • Placebo comparator
    control

    nitrate,beta blocker

    Drug: ticagrelor

  • Active comparator
    ticagrelor

    ticagrelor 90mg qd

    Drug: ticagrelor

Interventions

  • Drugticagrelor

    compare the effect of ticagrelor and control on the Coronary Flow Reserve in patients with microvessel angian

    Also known as: Brilinta

06

What researchers measure

Primary outcomes

  1. adenosine-induced coronary flow reserve (CFR)

    Time frame: 2 months

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 6, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02284048
Lead sponsor
Second Xiangya Hospital of Central South University
Responsible party
Daoquan Peng (Professor, Second Xiangya Hospital of Central South University) — Principal investigator
First posted
Nov 5, 2014
Start date
Nov 2014
Primary completion
Nov 2016 (estimated)
Completion
Nov 2017 (estimated)
Last update
Nov 6, 2014

Study contacts

Daoquan Peng, MD, PhD
Contact
pengdq@hotmail.com
86-731-85295806
Daoquan Peng, MD, PhD
study chair · Second Xiangya Hospital of Central South University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.

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