Coronary Artery DiseaseSTENT-FREENCT05222061
A Study of Drug Coated Balloon For Treating the Side Branch in Complex Bifurcation Lesions
A study testing Drug coated balloon for the side brunch and Conventional balloon for the side brunch in people with Coronary Artery Disease, run by Meshalkin Research Institute of Pathology of Circulation at 1 site in Russia.
Trial summary
Hypothesis: In patients undergoing coronary stenting for the true bifurcation lesions, main branch stenting followed by side branch dilatation with drug coated balloon is superior to the provisional-stenting strategy in terms of late lumen loss at 12 months. Read more about this study
- Who is it for?
- Ages 18 to 85 years
- Conditions the study is for
- Coronary Artery Disease
- What is being tested?
- Drug coated balloon for the side brunch and Conventional balloon for the side brunch
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteRussia
- Study dates
- 15 Feb 2022to 15 Feb 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 85 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Main branch and side branch diameter both >2.5 mm, evaluated based on coronary angiography, performed no later than 6 month before baseline visit;
- Patient ≥18 years old;
- Signed informed consent;
- True bifurcation lesion type 1:1:1 or 0:1:1 or 1:0:1 and
- ischemic symptoms, or
- positive non-invasive imaging for ischemia, or
- positive fractional flow reserve
Who cannot join
- ST Elevation Miocardial Infarction <72 hours preceding;
- Cardiogenic shock;
- Chronic total occlusion of either main or side branch of the bifurcation;
- >2 other coronary lesions planned for treatment;
- SYNTAX score >32;
- Left main stenosis;
Show all 11Show fewer
- In-stent restenosis;
- Renal function insufficiency: Serum creatinine > 177 mmol/l; or undergoing hemodialysis;
- Left ventricular ejection fraction ≤ 30%;
- Patient life expectancy less than 12 months;
- Patient's inability to fully cooperate with the study protocol
Trial locations and contacts
1 site in 1 country.
Russia1 site, 1 recruiting
- Recruiting
Meshalkin National Medical Research Center
Novosibirsk, Novosibirsk Oblast, 630055
Dmitrii Khelimskii, MD, PhD, +79137069256, dkhelim@mail.ru
Oleg Krestyaninov, MD, PhD
About this study
Official title: A ProSpecTivE, RaNdomIzed Trial of Drug Coated Balloon For tReating the Side
Hypothesis: In patients undergoing coronary stenting for the true bifurcation lesions, main branch stenting followed by side branch dilatation with drug coated balloon is superior to the provisional-stenting strategy in terms of late lumen loss at 12 months.
Read the detailed description
Although drug-eluting stents are still the default interventional treatment of coronary artery disease, drug-coated balloons (DCBs) represent an alternative therapeutic strategy in certain anatomic conditions. Although their use is established for in-stent restenosis of both bare-metal and drug-eluting stents, recent clinical data demonstrate promising results in de novo small-vessel disease, myocardial infarction and bifurcation settings.
Patients with coronary bifurcation lesions account for approximately 15% to 20% of all coronary lesions in coronary interventional procedures. Despite the use of drug-eluting stents, treating bifurcation lesions remains challenging especially in settings of side branch involvment. PCI of such lesions is associated with lower immediate angiographic and clinical success and higher rates of restenosis, which, in addition, are more challenging to treat compared to non-bifurcated lesions.
The optimal treatment of patients with biffurcations lesions involving SB is as yet undefined. Despite provisional stenting strategy is the preferred technique for most patients. Several studies demonstrated that two-stent techniques may be preferable in patients with true bifurcation lesions. However, as a general approach, the EBC suggests conducting PCI procedures with the aim of limiting the amount of stent metal implanted.
In this settings the use of DCB for bifurcation lesions may have some advantages. DCB provides a smaller profile compared with DES, allowing better SB access. The lack of foreign body implantation with DCB obviates the risk for stent thrombosis and may allow for a shorter duration of dual-antiplatelet therapy compared with DES.
To date, there have been very few clinical trials on the treatment of bifurcation lesions with drug-eluting balloons and all of these included only a small cohort of patients.
Early studies looking into the use of a BMS in the MB in combination with a DCB in the SB demonstrated a low late lumen loss in the SB when treated alone with a DCB [9]; recent observational studies focusing largely on a SB DCB combined with an MB DES strategy showed good SB results.
In the register PEPCAD V, 28 patients with lesions involving coronary bifurcation were treated by DCB Sequent Please in the secondary branch and the main vessel, BMS implantation in the main vessel, opening the stent struts toward the SD with only one balloon. At 9 months, the LLL in the MB was 0.38 ± 0.46 and 0.21 ± 0.48 mm in the SB resulting in an MLD of 2.2 ± 0.60 mm in the MB and 1.7 ± 0.44 mm in the SB. Three patients had angiographic restenosis, and in one a TLR was performed. Two patients experienced a late stent thrombosis at 6 and 8 months.
Improvement in the technique of intervention with the use of DES and DCB was observed in the prospective multicenter, non-randomized study DEBSIDE. Data from 50 patients were included,. Predilatation of both branches was performed with conventional balloons, then provisional stenting of MB using DES, kissing dilatation with conventional balloons. Authors proposed to remove guidewire from the MB in order to reduce the friction of the DCB and the loss of the antiproliferative drug from the surface of the balloon when it was delivered to the SB, to inflate the balloon with a pressure of 8-10 atmospheres for 30 seconds. Coronary angiography after 6 months, showed the LLL in the SB was 0.04 ± 0.34 mm, and in the MB, 0.54 ± 0.60 mm. The revascularization rate at 12 months was 6% and 2% in MB and SB, respectively.
A prospective multicenter study by Iannopollo G. analyzed results of the Agent DCB application in the real-world population. Among the 354 patients included in the registry (450 lesions treated with 508 DCBs), DCBs were used for the treatment of bifurcation lesions in 26%. DCB was inflated in the SB with a pressure of 8 atmospheres for 60 seconds after provisional stenting of the MB with the DES. The frequency of MACE after 544 days was 3.7%.
In the case of restenosis, DCB considered today a valuable alternative to DES, with strong evidence for the treatment of both BMS and DES restenosis. With its advantage of avoiding the creation of a dual stent layer in the coronary arteries, their use seems particularly attractive especially in patients with complex bifurcation lesions. In these settings DCB does seem to be a promising strategy, however, large randomised clinical trials are needed to show the safety and efficacy of this technology.
- Conditions
- Coronary Artery Disease
- Being tested
- Drug coated balloon for the side brunch, Conventional balloon for the side brunch
- Keywords
- Drug coated balloon, coronary bifurcation
- Medical subject headings
- Coronary Artery Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Drug coated balloon for the side brunchDevice
Intervention is explained in group description
Conventional balloon for the side brunchDevice
Intervention is explained in group description
| Study group | Role | What they receive |
|---|---|---|
| provisional-stenting group | Active comparator | Provisional stenting will be performed according to european bifurcation club consensus. MB and SB predilatation will be at the operator's discretion. A stent is delivered in the main vessel and positioned across the bifurcation. POT is mandatotary. In case of dissection impeding the flow in the SB or acute coronary closure after MB atenting a SB stenting using a DES was allowed. Dual-stent techniques will be performed according to the recommendation of the EBC consensus. Receives: Device: Conventional balloon for the side brunch |
| DCB group | Experimental | Coronary guidewires should be passed to the MB and SB, respectively. Lesion preparation of the main branch should be undertaken as considered necessary. Lesion preparation of the side branch is mandatorary. If the angiographic result will be good after predilatation (residual stenosis < 30%), drug-eluting stent will implanted in the main branch of the bifurcation site (the stent diameter should be choosen based on the diameter of the distal MB). A kissing with conventional balloons should be performed in the MB and SB. Reapet kissing with drug-coated balloonin the SB and conventional balloon in MB (30 seconds at low pressure (8-10 bar) should be performed. The DCB diameter was again 0.8-1.0 of the vessel diameter.
In case of dissection impeding the flow in the SB or acute coronary closure after DCB application a SB stenting using a DES was allowed. Dual-stent techniques will be performed according to the recommendation of the EBC consensus. Receives: Device: Drug coated balloon for the side brunch |
What is being measured
The primary outcome is the main question the study is designed to answer.
Late lumen loss for both main branch and side branch
Measured by quantitative coronary angiography.
Measured: 12 months
Secondary outcomes (9)
Major Adverse Cardiac Events (MACE)
Includes cardiac death, myocardial infarction in target vessel territory, clinically Indicated target lesion revascularization
Measured: 3,6,12 months
All-cause death
Measured: 3,6,12 months
Stent/vessel thrombosis
According to the definition of ARC (definite or probable)
Measured: 3,6,12 months
Angiographic Binary Restenosis
Measured by quantitative coronary angiography.
Measured: 12 months
Target Lesion Revascularization
TLR is defined as any ischemia-driven repeat PCI of the target lesion (including 5 mm proximal and distal to the target lesion) or bypass surgery of the target vessel.
Measured: 3,6,12 months
Target Vessel Revascularization
TVR as any ischemia-driven repeat PCI or bypass surgery of the target vessel. The target vessel consists of target lesion(s) and any additional lesions in the main epicardial coronary artery or branches containing the target lesion.
Measured: 3,6,12 months
Angina status
Change in the stable angina functional class according to Canadian Cardiovascular Society
Measured: 3,6,12 months
Angiographic success in main branch and side branch
Defined as a residual stenosis <30% and TIMI flow grade 3 at the end of the procedure in the MB and SB respectively
Measured: immediately after the procedure
Fluoroscopic time
Measured: immediately after the procedure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Feb 2022
- Study start15 Feb 2022 (estimated)
- Primary completion15 Feb 2023 (estimated)
- Study completion15 Feb 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Coronary Artery DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Meshalkin Research Institute of Pathology of Circulation
- Sponsor type
- Research network
- Responsible party
- Principal investigator, Dmitrii Khelimskii, Meshalkin Research Institute of Pathology of Circulation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05222061
- Sponsor's protocol ID
- 01-45
- Acronym
- STENT-FREE
- Status last verified
- Jan 2022
- First submitted
- 15 Apr 2021
- Last updated
- 3 Feb 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Feb 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A ProSpecTivE, RaNdomIzed Trial of Drug Coated Balloon For tReating the Side
- ClinicalTrials.gov ID
- NCT05222061
- Acronym / sponsor ID
- STENT-FREE / 01-45
- Conditions
- Coronary Artery Disease
- Keywords
- Drug coated balloon, coronary bifurcation
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Meshalkin Research Institute of Pathology of CirculationResearch network
- Study start
- 15 Feb 2022 (estimated)
- Primary completion
- 15 Feb 2023 (estimated)
- Study completion
- 15 Feb 2023 (estimated)
- First posted
- 3 Feb 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Hypothesis: In patients undergoing coronary stenting for the true bifurcation lesions, main branch stenting followed by side branch dilatation with drug coated balloon is superior to the provisional-stenting strategy in terms of late lumen loss at 12 months.
Detailed description
Although drug-eluting stents are still the default interventional treatment of coronary artery disease, drug-coated balloons (DCBs) represent an alternative therapeutic strategy in certain anatomic conditions. Although their use is established for in-stent restenosis of both bare-metal and drug-eluting stents, recent clinical data demonstrate promising results in de novo small-vessel disease, myocardial infarction and bifurcation settings.
Patients with coronary bifurcation lesions account for approximately 15% to 20% of all coronary lesions in coronary interventional procedures. Despite the use of drug-eluting stents, treating bifurcation lesions remains challenging especially in settings of side branch involvment. PCI of such lesions is associated with lower immediate angiographic and clinical success and higher rates of restenosis, which, in addition, are more challenging to treat compared to non-bifurcated lesions.
The optimal treatment of patients with biffurcations lesions involving SB is as yet undefined. Despite provisional stenting strategy is the preferred technique for most patients. Several studies demonstrated that two-stent techniques may be preferable in patients with true bifurcation lesions. However, as a general approach, the EBC suggests conducting PCI procedures with the aim of limiting the amount of stent metal implanted.
In this settings the use of DCB for bifurcation lesions may have some advantages. DCB provides a smaller profile compared with DES, allowing better SB access. The lack of foreign body implantation with DCB obviates the risk for stent thrombosis and may allow for a shorter duration of dual-antiplatelet therapy compared with DES.
To date, there have been very few clinical trials on the treatment of bifurcation lesions with drug-eluting balloons and all of these included only a small cohort of patients.
Early studies looking into the use of a BMS in the MB in combination with a DCB in the SB demonstrated a low late lumen loss in the SB when treated alone with a DCB [9]; recent observational studies focusing largely on a SB DCB combined with an MB DES strategy showed good SB results.
In the register PEPCAD V, 28 patients with lesions involving coronary bifurcation were treated by DCB Sequent Please in the secondary branch and the main vessel, BMS implantation in the main vessel, opening the stent struts toward the SD with only one balloon. At 9 months, the LLL in the MB was 0.38 ± 0.46 and 0.21 ± 0.48 mm in the SB resulting in an MLD of 2.2 ± 0.60 mm in the MB and 1.7 ± 0.44 mm in the SB. Three patients had angiographic restenosis, and in one a TLR was performed. Two patients experienced a late stent thrombosis at 6 and 8 months.
Improvement in the technique of intervention with the use of DES and DCB was observed in the prospective multicenter, non-randomized study DEBSIDE. Data from 50 patients were included,. Predilatation of both branches was performed with conventional balloons, then provisional stenting of MB using DES, kissing dilatation with conventional balloons. Authors proposed to remove guidewire from the MB in order to reduce the friction of the DCB and the loss of the antiproliferative drug from the surface of the balloon when it was delivered to the SB, to inflate the balloon with a pressure of 8-10 atmospheres for 30 seconds. Coronary angiography after 6 months, showed the LLL in the SB was 0.04 ± 0.34 mm, and in the MB, 0.54 ± 0.60 mm. The revascularization rate at 12 months was 6% and 2% in MB and SB, respectively.
A prospective multicenter study by Iannopollo G. analyzed results of the Agent DCB application in the real-world population. Among the 354 patients included in the registry (450 lesions treated with 508 DCBs), DCBs were used for the treatment of bifurcation lesions in 26%. DCB was inflated in the SB with a pressure of 8 atmospheres for 60 seconds after provisional stenting of the MB with the DES. The frequency of MACE after 544 days was 3.7%.
In the case of restenosis, DCB considered today a valuable alternative to DES, with strong evidence for the treatment of both BMS and DES restenosis. With its advantage of avoiding the creation of a dual stent layer in the coronary arteries, their use seems particularly attractive especially in patients with complex bifurcation lesions. In these settings DCB does seem to be a promising strategy, however, large randomised clinical trials are needed to show the safety and efficacy of this technology.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| provisional-stenting group | Active comparator | Device: Conventional balloon for the side brunchProvisional stenting will be performed according to european bifurcation club consensus. MB and SB predilatation will be at the operator's discretion. A stent is delivered in the main vessel and positioned across the bifurcation. POT is mandatotary. In case of dissection impeding the flow in the SB or acute coronary closure after MB atenting a SB stenting using a DES was allowed. Dual-stent techniques will be performed according to the recommendation of the EBC consensus. |
| DCB group | Experimental | Device: Drug coated balloon for the side brunchCoronary guidewires should be passed to the MB and SB, respectively. Lesion preparation of the main branch should be undertaken as considered necessary. Lesion preparation of the side branch is mandatorary. If the angiographic result will be good after predilatation (residual stenosis < 30%), drug-eluting stent will implanted in the main branch of the bifurcation site (the stent diameter should be choosen based on the diameter of the distal MB). A kissing with conventional balloons should be performed in the MB and SB. Reapet kissing with drug-coated balloonin the SB and conventional balloon in MB (30 seconds at low pressure (8-10 bar) should be performed. The DCB diameter was again 0.8-1.0 of the vessel diameter. In case of dissection impeding the flow in the SB or acute coronary closure after DCB application a SB stenting using a DES was allowed. Dual-stent techniques will be performed according to the recommendation of the EBC consensus. |
Who may qualify
- Ages
- 18 to 85 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Main branch and side branch diameter both >2.5 mm, evaluated based on coronary angiography, performed no later than 6 month before baseline visit;
- Patient ≥18 years old;
- Signed informed consent;
- True bifurcation lesion type 1:1:1 or 0:1:1 or 1:0:1 and
- ischemic symptoms, or
Key exclusion criteria (11 listed)
- ST Elevation Miocardial Infarction <72 hours preceding;
- Cardiogenic shock;
- Chronic total occlusion of either main or side branch of the bifurcation;
- >2 other coronary lesions planned for treatment;
- SYNTAX score >32;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Drug coated balloon for the side brunchIntervention is explained in group description | Device | DCB group |
| Conventional balloon for the side brunchIntervention is explained in group description | Device | provisional-stenting group |
Primary outcome
Late lumen loss for both main branch and side branch
Time frame: 12 months
Measured by quantitative coronary angiography.
9 secondary outcomes
Major Adverse Cardiac Events (MACE)
Time frame: 3,6,12 months
All-cause death
Time frame: 3,6,12 months
Stent/vessel thrombosis
Time frame: 3,6,12 months
Angiographic Binary Restenosis
Time frame: 12 months
Target Lesion Revascularization
Time frame: 3,6,12 months
Target Vessel Revascularization
Time frame: 3,6,12 months
Angina status
Time frame: 3,6,12 months
Angiographic success in main branch and side branch
Time frame: immediately after the procedure
Fluoroscopic time
Time frame: immediately after the procedure
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Feb 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Drug coated balloon for the side brunch and Conventional balloon for the side brunch in people with Coronary Artery Disease, run by Meshalkin Research Institute of Pathology of Circulation at 1 site in Russia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 3 Feb 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Russia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Dmitrii Khelimskii, MD, PhD (+79137069256, dkhelim@mail.ru), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Late lumen loss for both main branch and side branch (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Feb 2022.