Transcatheter Edge-to-Edge Repair In Moderate and Exertional-Induced Severe MR (TIMER)

Trial statusNot yet recruiting
Trial phaseEarly Phase 1
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorSun Yat-sen University

About this trial

Transcatheter Edge-to-Edge Repair (TEER) has become an established alternative for the treatment of severe mitral regurgitation (MR). RESHAPE trial indicated that patients with moderate functional MR (FMR) and heart failure (HF) might benefit from TEER. However, it still not clear that TEER is effective for which subset of patients with FMR.

Hand-Gripping (HG), characterized with an increased venous return, preservation or increase of left ventricular (LV) afterload and systemic vascular resistance, has been identified as a means of stress test to identify exertion-induced mitral regurgitation. Most importantly, compared to exercise stress testing via treadmill running or cycling in patients with moderate FMR, HG demonstrates significantly higher feasibility and safety.

HG-induced severe MR reflects the reversibility of the regurgitation under stress, suggesting that reducing MR through TEER might alleviate LV volume overload, improve cardiac efficiency, and mitigate symptoms, which need to be validated in this trial.

TIMER is a multi-center, randomized, double blind, placebo-controlled trial. A total of 300 patients with moderate and exertional-induced severe MR will be randomized in a 1:1 ratio to the treatment with TEER and guideline-directed medical therapy (GDMT) or GDMT only.

The primary endpoint of this study is rehospitalization within 24 months.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Moderate functional mitral regurgitation

HG-induced severe functional mitral regurgitation

Left ventricular ejection fraction (LVEF) between 20% to 50%

Left ventricular end-systolic diameter (LVESD) ≤70 mm

Disqualifiers

Stage D heart failure per ACC/AHA guidelines with hemodynamic instability or cardiogenic shock

Untreated symptomatic coronary artery disease requiring revascularization

Chronic obstructive pulmonary disease (COPD) requiring continuous oxygen therapy or long-term corticosteroids therapy

Severe pulmonary hypertension or moderate-to-severe right ventricular dysfunction

Trial design

Design model

Parallel

Treatments tested in this trial

  • TEER

    Device

    TEER

  • GDMT

    Drug

    GDMT

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: TEERExperimental treatment 2 interventions
Group B: Control groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Rehospitalization rate

Rehospitalization rate within 24 months

Time frame
24 months

Secondary outcomes

1

KCCQ

Range of 0-100, with higher scores indicating better health status

Time frame
24 months
2

NYHA class

I-IV

Time frame
24 months
3

6-min walk test

\>500 m: Normal exercise capacity 350-500 m: Mild impairment 150-350 m: Moderate impairment \<150 m: Severe impairment

Time frame
24 months
4

MACE

Cardiovascular Death, Myocardial Infarction, Stroke

Time frame
24 months

Other outcomes

1

Safety Outcome

Complications of TEER

Time frame
24 months

Sponsors and contacts

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