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Isosorbide mononitrate reduces composite events (OR 0.74) in patients with lacunar strokeTrial Shows Isosorbide Mononitrate Reduces Risks After Lacunar Stroke

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Key Takeaway
Consider isosorbide mononitrate as a potential treatment to reduce composite events in lacunar stroke patients.

This Phase 2b randomized trial enrolled 363 participants aged over 30 years with clinical lacunar stroke and compatible neuroimaging. The study aimed to evaluate the efficacy of isosorbide mononitrate (40-60 mg) or cilostazol (200 mg) compared to a control group over a 6-month follow-up period.

Primary outcomes included a composite of stroke, myocardial infarction, dependency (modified Rankin Scale score >2), cognitive impairment (version 5, 7-level >0), and death. Patients receiving isosorbide mononitrate showed fewer composite events compared to the control group (OR 0.74; 95% CI, 0.55-0.99). Additionally, isosorbide mononitrate was associated with improved stroke impact (-0.15; 95% CI -0.25 to -0.05).

Secondary outcomes showed that cilostazol improved cognition (OR 0.64; 95% CI, 0.41-0.99) compared to control. Both isosorbide mononitrate and cilostazol were associated with improved cognition (OR 0.40; 95% CI, 0.21-0.78) and improved mood (-6.94; 95% CI, -12.25 to -1.64) compared to control. Global stroke impact was also improved in the combined treatment group (-0.23; 95% CI, -0.37 to -0.09).

Safety data and tolerability were not reported. The study utilized an open-label design, which may limit certain interpretations of the results. As a Phase 2b trial, these findings serve as proof-of-concept for managing complications in cerebral small vessel disease.

How this fits prior evidence

How this fits prior evidence: This study addresses a gap identified in a previous narrative review that discussed cerebral small vessel disease without reporting specific interventions or outcomes. While earlier evidence established that higher m-cSVD scores are linked to increased stroke risk and that certain genetic markers relate to cerebral small vessel disease phenotypes, this trial provides specific intervention data for lacunar stroke patients.

Researchers conducted a Phase 2b trial to see how two different medications, isosorbide mononitrate and cilostazol, affected people over age 30 who had suffered a lacunar stroke. This type of study is designed as a proof-of-concept to see if these treatments show potential for further testing.

The study found that patients taking isosorbide mononitrate had fewer composite events, such as new strokes or heart attacks, compared to those in the control group. These patients also showed improvements in their daily stroke impact scores. Meanwhile, patients taking cilostazol or a combination of both medications showed improved cognitive scores and better moods.

Because this was a Phase 2b trial with an open-label design, the results are preliminary. The study focused on a short follow-up period of six months. These findings show promise for these treatments in managing stroke impacts, but more large-scale research is needed to confirm these effects and ensure long-term safety.

What this means for you:
Isosorbide mononitrate and cilostazol showed potential benefits for stroke recovery in this early-stage trial.

Common questions

What did the study find regarding isosorbide mononitrate?

The trial found that patients taking isosorbide mononitrate had fewer composite events, which included new strokes, heart attacks, and physical dependency. These patients also showed improved scores regarding their daily stroke impact compared to those who did not take the medication.

How did cilostazol affect cognitive health?

Patients taking cilostazol showed improved cognition on a 7-level scale. Those taking a combination of both isosorbide mononitrate and cilostazol also showed significant improvements in cognitive scores compared to the control group.

What other benefits were noted for patients?

Patients taking either medication or a combination of both showed improved mood scores and better global stroke impact. These results were observed during the six-month follow-up period after starting the treatment.

Study Details

Study typeRct
Sample sizen = 363
EvidenceLevel 2
Follow-up6.0 mo
PublishedAug 2026
View Original Abstract ↓
BACKGROUND: Lacunar stroke can cause cognitive decline and dependency. The LACI-2 (Lacunar Intervention Trial-2) trial showed that 12 months of treatment with isosorbide-mononitrate (ISMN) or cilostazol improved these outcomes. We tested whether this effect was present at 6 months. METHODS: LACI-2 was a prospective randomized open-label blinded-end point 2×2-factorial phase-2b trial assessing feasibility, safety, and proof-of-concept of 1 year of ISMN (40-60 mg) or cilostazol (200 mg). Participants aged >30 years had clinical lacunar stroke, compatible neuroimaging, and capacity to consent. The primary clinical outcome was the composite of stroke, myocardial infarction, dependency (modified Rankin Scale score >2), cognitive impairment ( version 5, 7-level >0) and death; key secondary outcomes included the composite components, mood and stroke impact scale. Global analysis of the stroke impact scale was analyzed using the Wei-Lachin test with result given as Mann-Whitney difference. RESULTS: Baseline characteristics were balanced across 363 participants: median age 64 (56-72) years, 31% female, and median onset to randomization 79 (27-244) days. At 6 months, participants allocated to ISMN versus control had fewer composite events (adjusted odds ratio [OR], 0.74 [95% CI, 0.55-0.99]) and improved stroke impact (Mann-Whitney difference, -0.15 [95% CI -0.25 to -0.05]). Cilostazol versus control improved cognition ( version 5, 7-level scale, adjusted common OR, 0.64 [95% CI, 0.41-0.99]). ISMN/cilostazol versus control improved cognition ( version 5, 7-level adjusted common OR, 0.40 [95% CI, 0.21-0.78]), mood (Zung adjusted mean difference, -6.94 [95% CI, -12.25 to -1.64]) and global stroke impact (Mann-Whitney difference, -0.23 [95% CI, -0.37 to -0.09]). CONCLUSIONS: A reduction in the composite outcome, cognitive impairment, dependency, and stroke impact was seen within 6 months of starting ISMN or cilostazol. REGISTRATION: URL: www.isrctn.com; Unique Identifier: ISRCTN14911850.
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