Conventional Versus Intentional StraTegy in Lesions With High Risk PrEdiction of Side Branch OccLusion in InterVEntion

1. Statistical Design and Analysis. 1.1 Analysis Population(s). 1.1.1 Intent to Treat Population (ITT, primary clinical endpoint only). The ITT population set will consist of all subjects who signed the written informed consent and are randomized, regardless which strategy was selected. The primary analysis is a superiority ITT analysis of the primary clinical endpoint, being side branch occlusion after main vessel stenting. 1.1.2 Per Protocol (PP, for clinical endpoints). If required, an additional analysis of the Per-Protocol (PP) population will be conducted of the primary and secondary endpoints. The PP population consists of those subjects who correctly received (only) the assigned study stent. Should all subjects correctly receive (only) the assigned study stent(s), no PP analysis will be required for the clinical endpoints. 1.2 Statistical Methods. 1.2.1 Statistical Hypothesis for the Primary Endpoint. H0: Pt-Pc ≥0; H1: Pt-Pc <0; where Pt and Pc are the rates of side branch occlusion in the intentional strategy (test) and convention strategy (control) groups, respectively. The study is powered at 80% to show differences in the rate of side branch occlusion between intentional strategy group and conventional strategy group. The primary analysis will be performed for the ITT patient population. 1.2.2 Statistical Test Method for the Primary Endpoint. Normal approximation test for the difference between two proportions (pooled proportion) or Fisher's exact test (if applicable) will be used to test the two-sided hypothesis of superiority in proportions. If the P value from the two-sided test is <0.05, the intentional strategy (test) will be concluded to be superior to conventional strategy. This corresponds to the two-sided upper 95% confidence bound on the difference between treatment groups in side branch occlusion (the intentional strategy - conventional strategy) being less than delta. 1.2.3 Sample Size Parameters for the Primary Endpoint.

• A 1:1 treatment allocation ratio of intentional strategy group and the conventional strategy group
• A two-side significance level (alpha) of 0.05
• 80% power to show differences in the rate of side branch occlusion between intentional strategy group and conventional strategy group
• The rate of side branch occlusion in intentional strategy group: 4.0%
• The rate of side branch occlusion in conventional strategy group: 10.0%
• The primary endpoint would be reached immediately after the main vessel stenting, therefore, the attrition rate is 0% The 10% rate of side branch occlusion in conventional strategy group is based on the V-RESOLVE study. It is reasonable to assume that, with an intentional strategy for bifurcation lesions with V-RESOLVE score ≥12 points, the rate of side branch occlusion would decrease to 4% in intentional strategy group. Thus, the present study requires 283 subjects in intentional strategy group and 283 in conventional strategy group, and the total number will be 566. 1.3 Secondary Endpoint Analysis. For all secondary endpoints the results of the intentional strategy and conventional strategy groups will be compared. For clinical endpoint the analysis will be performed at each follow-up visit, meaning at 1 Month, 3 Months, 6 Months and 12 Months. The analysis will be performed for the ITT population and, if applicable, the PP population. For all secondary endpoints conventional p-values and 95% confidence intervals for the difference in Kaplan-Meier will be calculated. Dichotomous variables will be evaluated using Fisher's exact tests. Continuous variables will be evaluated by a two-sample t-test, a 95% confidence interval and p-value will be reported. For time-dependent analyses, Hazard Ratios will be evaluated using Cox proportional hazards model and Kaplan Meier estimates will be evaluated according to log-rank test. 1.4 Missing Data. Every effort will be undertaken to minimize missing data. The following approach to handling missing data will be adopted based on the type of the outcome and endpoint being analyzed. Kaplan-Meier estimates will censor incomplete data at the last date of available follow-up information, assuming complete reporting of all events up to that date and event status unknown after that date. 1.5 Calculating Days to Event. When calculating the days-to-event, the date the event took place will always be compared to the index procedure date, also in case a staged procedure took place. 1.6 Within Patient Correlation. In case for a patient more than one lesion will be analyzed, in-patient correlation will be taken into account.

1. Study Data Reporting, Monitoring and Quality Assurance.

2.1 Data Recording.

The data collection tool for this study is a validated electronic data capture system that contains a system generated audit trail. Data required according to this protocol are recorded by investigational site personnel via data entry into the internet based Electronic Data Capture (EDC) software system. All internal and external investigational site personnel seeking access must go through a training process before they are granted access to the electric Case Report Form (eCRF). Training records are maintained. All personnel with access to the eCRF are supported by a Service Desk (if applicable).

Clinical data management will be performed in accordance with applicable sponsor's/Clinical Research Organization (CRO)'s standards and data cleaning procedures. This is applicable for data recorded in the eCRF as well as for data from other sources (e.g. laboratory, ECG, adjudication committees).

Edit checks and queries will be built into the EDC application as described in the Data Management Plan. Queries generated by rules and raised by reviewers will be generated and resolved within the EDC application. During this review, subject data will be checked for consistency, omissions, and any apparent discrepancies.

All Adverse Events, medication and medical histories (if applicable) will be coded using Medical Dictionary for Regulatory Activities (MedDRA).

Data received from external sources such as central labs will be reconciled to the clinical database.

Serious Adverse Events in the clinical database will be reconciled with the safety database.

2.2 Source Documentation.

It is the investigator's responsibility that data entries made in the eCRF are supported by source documents maintained for all subjects enrolled in this study.

Source documents include all recordings and observations or notations of clinical activities and all reports and records necessary for the evaluation of the clinical study. The site must implement processes to ensure availability of all required source documentation.

2.3 Monitoring.

Monitoring the clinical investigation at the study site is the responsibility of the monitoring organization through trained and qualified Clinical Research Associates (CRAs). Monitoring will be performed as described in the Monitoring Plan.

2.4 Audit and Inspection.

To ensure compliance with Good Clinical Practices (GCP) and regulatory requirements, a member of the sponsor's (or a designated CRO's) quality assurance unit may arrange to conduct audits to assess the performance of the study at the study sites and of the study documents originating there. The investigator/institution will be informed of the audit outcome.

In addition, inspections by regulatory health authority representatives and Institutional Review Board (IRB) are possible. The investigator should notify the sponsor immediately of any such inspection.

The investigator/institution agrees to allow the auditor or inspector direct access to all relevant documents and allocate his/her time and the time of his/her staff to the auditor/inspector to discuss findings and any issues. Audits and inspections may occur at any time during or after completion of the study.

In accordance with GCP and the Sponsor's audit plans, this study may be selected for audit by representatives from Sponsor. Inspection of site facilities (e.g., pharmacy, Device storage areas, laboratories etc.) and review of study related records will occur in order to evaluate the study conduct and compliance with the protocol, GCP, and applicable regulatory requirements.

2.5 Archiving.

All Case Report Forms (CRFs), study records, reports and source documents that support the CRFs must be retained in the files of the responsible Investigators for a minimum 2 years following notification by the Sponsor or designee that all investigations have been completed, and will further be retained in accordance with local and international guidelines as identified in the clinical study agreement. This documentation must be accessible upon request by international regulatory authorities, the Sponsor (or designee). The sponsor or designee, must approve archiving or transfer of the documentation for relocation purpose of premises, in writing, prior to the actual file transfer. The investigator must notify the Sponsor, in writing, of transfer location, duration, and the procedure for accessing study documentation. The Investigator must contact the Sponsor, or designee, before the destruction of any records and reports pertaining to the study to ensure they no longer need to be retained.

If the Investigator retires, relocates, or for other reasons withdraws from assuming primary responsibility for keeping the study records, custody per written notice must be submitted to the Sponsor, or designee, indicating the name and address of the person accepting primary responsibility. The Ethics Committee (EC) must be notified in writing of the name and address of the new custodian.

2.6 Deviations from Protocol.

A protocol deviation is defined as an event where the study is not conducted according to the protocol and applicable regulations. Protocol deviations that will be collected include, but are not limited to the following:

• Failure to obtain informed consent or failure to obtain informed consent prior to study procedures;
• Enrolling a subject who did not meet inclusion criteria, or met exclusion criteria;
• Not completing protocol-required examinations or evaluations.

A Protocol Deviation eCRF needs to be completed separately for each type of deviation and submitted to the Sponsor and any reviewing Regulatory Body, such as the EC as required.

Protocol deviations are reportable to the Sponsor as soon as possible after their occurrence.

2.6.1 Site Non-Compliance.

If excessive protocol deviations are noted, the Sponsor reserves the right to suspend study enrollment until a sufficient system is in place at the site to reduce further deviations, or to withdraw the site from participation in the study.

2.7 Compliance to Standard Regulations.

The protocol, informed consent form and other study-related documents will be submitted to the EC / IRB. The study will be performed in accordance with the Declaration of Helsinki and GCP.

The trial will only start at a clinical site after written approval of the study has been obtained from the appropriate national EC/IRB.