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A Network Meta-analysis of Angiotensin Receptor-Neprilysin Inhibitors and Cancer Risk Based on Parallel-Group Individual Randomized Controlled Trials

A Network Meta-analysis of Angiotensin Receptor-Neprilysin Inhibitors and Cancer Risk Based on Parallel-Group Individual Randomized Controlled Trials - A Network Meta-analysis of Angiotensin Receptor-Neprilysin Inhibitors and Cancer Risk Based on Parallel-Group Individual Randomized Controlled Trials

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000060251
Enrollment
Unknown
Registered
2026-01-12
Start date
2026-01-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Coronary artery disease, Heart failure, Chronic kidney disease, Atrial fibrillation, High risk vascular disease, Cerebrovascular accident, Diabetes mellitus, High normal blood pressure, Pre-hypertension

Interventions

None listed

Sponsors

Yokohama City University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: We will include only English full-articles. The other article including non-English article, short article, and conference abstract will be excluded. We will include parallel-group individual RCTs but not cluster RCTs, or cross-over RCTs. A trial with three or more arms will be accepted. Along with superiority trials, non-inferiority trials will be allowed. Any phase RCT may be included. Trials not reporting data about safety outcomes will be excluded. Key inclusion criteria are as follows. (1) RCTs including RAS-acting agents and control treatment in adult patients. Controls will be classified as placebo or non-placebo. Non-placebo drugs will be defined as any RAS-acting agents. (2) The study with multiple arms where RAS-acting agent is included at least one arm. (3) The study illustrates the safety outcome of cancer.

Exclusion criteria

Exclusion criteria: (1) Systematic review or meta-analysis articles. (2) Retrospective analysis. (3) Single prospective cohort study without a control group. (4) Non-RCT. (5) The republished research literature is excluded unless the research includes new findings related to cancers listed in inclusion criteria. (6) Studies with no or insufficient safety outcomes at the time of the literature search. Two investigators independently will screen all titles, abstracts, and full texts for eligibility. Final inclusion will be decided after resolving discrepancies between the two investigators.

Design outcomes

Primary

MeasureTime frame
The odds ratio (OR) of cancer with ARNI will be calculated. Network meta-analysis will be performed to compare the incidence of cancer between ARNI and control treatment. We will use five comparison categories: placebo, ARNI, angiotensin-converting-enzyme inhibitors (ACEi), angiotensin-receptor blockers (ARBs), ACEi and ARBs.

Secondary

MeasureTime frame
The odds ratio (OR) of cancer with ACEi, ARBs, ACEi and ARBs will be calculated. The main analysis will be compared individual drug classes with placebo, which will be used as reference.

Countries

Japan

Contacts

Public ContactShintaro Minegishi

Yokohama City University Graduate School of Medicine Department of Cardiology

minegishi.shi.fb@yokohama-cu.ac.jp0457872800

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026