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NCT05712746Active, not recruiting

Samtasu Post-marketing General Drug Use-results Survey in Patients With Volume Overload in Heart Failure.

Source: ClinicalTrials.gov · Last updated 22 Jun 2026

Brief summary (registry, in English)

To confirm the safety of tolvaptan sodium phosphate in patients with volume overload in heart failure.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1600 (estimated)
First submitted
16 Jan 2023
Start date
3 Mar 2023
Primary completion date
7 May 2026
Lead sponsor
Otsuka Pharmaceutical Co., Ltd.
NCT number
NCT05712746

What you commit to

  • Study type: Observational
  • Planned participants: 1600
  • From 3 Mar 2023 to the primary completion date, 7 May 2026
  • 1 site 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.

Lab values

  • patients with a known hypersensitivity to Tolvaptan sodium phosphate or Tolvaptan

Who the study is looking for

  • \-

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Pharmacovigilance Department
Coordinator of this site? Confirm its status
OsakaJapanUnknown status

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