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NCT Number: NCT07197021

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

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.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

The First Affiliated Hospital of Sun Yat-sen University

Guangzhou, Guangdong, 510080, China

Location contact

Xiaodong Zhuang

CONTACT

[email protected]

020-89998001

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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
  • Aortic or tricuspid valve disease requiring surgical or transcatheter intervention
  • Life expectancy <12 months

Treatment and study plan

TEER

Device

TEER

GDMT

Drug

GDMT

Primary outcomes

  1. Rehospitalization rate

    Time frame: 24 months

    Rehospitalization rate within 24 months

Secondary outcomes

  1. KCCQ

    Time frame: 24 months

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

  2. NYHA class

    Time frame: 24 months

    I-IV

  3. 6-min walk test

    Time frame: 24 months

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

  4. MACE

    Time frame: 24 months

    Cardiovascular Death, Myocardial Infarction, Stroke

Other outcomes

  1. Safety Outcome

    Time frame: 24 months

    Complications of TEER

Study contacts

Contact information is provided by the study sponsor or research team.

Xiaodong Zhuang, MD

CONTACT

[email protected]

020-89998001

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2030
First posted
Sep 29, 2025
Registry last updated
Sep 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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