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NCT05976230Completed

Special Drug Use Surveillance of Entresto Tablets (Hypertension)

Special Drug Use Surveillance of Entresto Tablets (Hypertension, CLCZ696A1402): ENLIGHT

Source: ClinicalTrials.gov · Last updated 16 Jun 2026

Brief summary (registry, in English)

This is a single arm, multicenter, observational study to evaluate the safety and efficacy of Entresto Tablets during the first 52 weeks of treatment in Japanese patients with hypertension.

Status (registry)
Completed
Study type
Observational
Enrollment
1125 (actual)
First submitted
28 Jul 2023
Start date
4 Sept 2023
Primary completion date
29 May 2025
Lead sponsor
Novartis Pharmaceuticals
NCT number
NCT05976230

What you commit to

  • Study type: Observational
  • Participants enrolled: 1125
  • From 4 Sept 2023 to the primary completion date, 29 May 2025
  • 84 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have received a formulation containing the same ingredient as Entresto (including investigational product or post-marketing clinical study drug)
  • The following patients for whom administration of Entresto is contraindicated in the package insert:
    • Patients with a history of hypersensitivity to any of the ingredients of Entresto
    • Patients who are receiving angiotensin-converting enzyme inhibitors (alacepril, imidapril hydrochloride, enalapril maleate, captopril, quinapril hydrochloride, cilazapril hydrate, temocapril hydrochloride, delapril hydrochloride, trandolapril, benazepril hydrochloride, perindopril erbumine, and lisinopril hydrate) or who discontinued these drugs within 36 hours.
    • Patients with a history of angioedema (angioedema due to angiotensin II receptor antagonists or angiotensin converting enzyme inhibitors, hereditary angioedema, acquired angioedema, idiopathic angioedema, etc.)
    • Patients with diabetes mellitus who are receiving aliskiren fumarate
    • Patients with severe hepatic impairment (Child-Pugh class C)
    • Pregnant or possibly pregnant women
  • Patients who have been hospitalized at the start of treatment with Entresto

Other illness

  • Patients with a history or complication of cardiac failure

Who the study is looking for

  • Patients who have given written consent to participate in this study before the start of treatment with Entresto
  • Patients who used Entresto for the first time for the indication of hypertension

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (84)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Novartis Investigative Site
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Aiko-gunJapanUnknown status
Novartis Investigative Site
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AkashiJapanUnknown status
Novartis Investigative Site
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AkishimaJapanUnknown status
Novartis Investigative Site
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AmagasakiJapanUnknown status
Novartis Investigative Site
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AnjoJapanUnknown status
Novartis Investigative Site
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AsakaJapanUnknown status
Novartis Investigative Site
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BandōJapanUnknown status
Novartis Investigative Site
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ChikuseiJapanUnknown status
Novartis Investigative Site
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Edogawa-kuJapanUnknown status
Novartis Investigative Site
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FujiminoJapanUnknown status
Novartis Investigative Site
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FujisawaJapanUnknown status
Novartis Investigative Site
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FukuokaJapanUnknown status
Novartis Investigative Site
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GyōdaJapanUnknown status
Novartis Investigative Site
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HachiōjiJapanUnknown status
Novartis Investigative Site
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HirakataJapanUnknown status
Novartis Investigative Site
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HiroshimaJapanUnknown status
Novartis Investigative Site
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IchinomiyaJapanUnknown status
Novartis Investigative Site
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IkedaJapanUnknown status
Novartis Investigative Site
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IkiJapanUnknown status
Novartis Investigative Site
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InzaiJapanUnknown status
Novartis Investigative Site
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KagoshimaJapanUnknown status
Novartis Investigative Site
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KanazawaJapanUnknown status
Novartis Investigative Site
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KasaiJapanUnknown status
Novartis Investigative Site
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KashimaJapanUnknown status
Novartis Investigative Site
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KasugaJapanUnknown status
Novartis Investigative Site
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KasugaiJapanUnknown status
Novartis Investigative Site
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Kasuya GunJapanUnknown status
Novartis Investigative Site
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Katsushika-kuJapanUnknown status
Novartis Investigative Site
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KawaguchiJapanUnknown status
Novartis Investigative Site
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Kishima-gunJapanUnknown status
Novartis Investigative Site
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KitakyushuJapanUnknown status
Novartis Investigative Site
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KobeJapanUnknown status
Novartis Investigative Site
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KogaJapanUnknown status
Novartis Investigative Site
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KokubunjiJapanUnknown status
Novartis Investigative Site
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Koto KuJapanUnknown status
Novartis Investigative Site
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KumamotoJapanUnknown status
Novartis Investigative Site
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KurashikiJapanUnknown status
Novartis Investigative Site
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KurumeJapanUnknown status
Novartis Investigative Site
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MachidaJapanUnknown status
Novartis Investigative Site
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MatsudoJapanUnknown status
Novartis Investigative Site
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MatsuyamaJapanUnknown status
Novartis Investigative Site
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MinohJapanUnknown status
Novartis Investigative Site
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MitakaJapanUnknown status
Novartis Investigative Site
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MoriguchiJapanUnknown status
Novartis Investigative Site
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MoriyaJapanUnknown status
Novartis Investigative Site
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NagasakiJapanUnknown status
Novartis Investigative Site
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NagoyaJapanUnknown status
Novartis Investigative Site
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NakagawaJapanUnknown status
Novartis Investigative Site
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NakatsuJapanUnknown status
Novartis Investigative Site
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NiizaJapanUnknown status
Novartis Investigative Site
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NishinomiyaJapanUnknown status
Novartis Investigative Site
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ŌbuJapanUnknown status
Novartis Investigative Site
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ŌitaJapanUnknown status
Novartis Investigative Site
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OkazakiJapanUnknown status
Novartis Investigative Site
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OmutaJapanUnknown status
Novartis Investigative Site
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OsakaJapanUnknown status
Novartis Investigative Site
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Ōta-kuJapanUnknown status
Novartis Investigative Site
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RyūgasakiJapanUnknown status
Novartis Investigative Site
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SaijōJapanUnknown status
Novartis Investigative Site
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SaitamaJapanUnknown status
Novartis Investigative Site
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SakuraJapanUnknown status
Novartis Investigative Site
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SapporoJapanUnknown status
Novartis Investigative Site
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SatteJapanUnknown status
Novartis Investigative Site
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SayamaJapanUnknown status
Novartis Investigative Site
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Setagaya-kuJapanUnknown status
Novartis Investigative Site
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Shibuya CityJapanUnknown status
Novartis Investigative Site
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ShimonosekiJapanUnknown status
Novartis Investigative Site
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SuitaJapanUnknown status
Novartis Investigative Site
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TakaokaJapanUnknown status
Novartis Investigative Site
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TakatsukiJapanUnknown status
Novartis Investigative Site
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TakeharaJapanUnknown status
Novartis Investigative Site
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TokorozawaJapanUnknown status
Novartis Investigative Site
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Toshima-KuJapanUnknown status
Novartis Investigative Site
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TosuJapanUnknown status
Novartis Investigative Site
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ToyohashiJapanUnknown status
Novartis Investigative Site
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ToyonakaJapanUnknown status
Novartis Investigative Site
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UreshinoJapanUnknown status
Novartis Investigative Site
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YamagaJapanUnknown status
Novartis Investigative Site
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YamaguchiJapanUnknown status
Novartis Investigative Site
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YameJapanUnknown status
Novartis Investigative Site
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YatomiJapanUnknown status
Novartis Investigative Site
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YokohamaJapanUnknown status
Novartis Investigative Site
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YokosukaJapanUnknown status
Novartis Investigative Site
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YotsukaidōJapanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.