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NCT07438925Active, not recruiting

Copeptin Concentration Measured in Plasma Samples and Intradialytic Blood Pressure Variation

Source: ClinicalTrials.gov · Last updated 27 Feb 2026

Brief summary (registry, in English)

Vasopressin is a key regulator of water and vascular homeostasis, acting through V2 receptors to control renal water reabsorption and through V1a receptors to influence vascular tone. Copeptin, a stable surrogate marker of vasopressin release, provides a reliable measure of vasopressin activity. In hemodialysis, where ultrafiltration and osmotic shifts challenge fluid balance, the contribution of vasopressin to intradialytic blood pressure regulation remains uncertain. Elevated copeptin levels in dialysis patients have been associated with interdialytic weight gain and adverse cardiovascular outcomes. This study (CODIALHYP) tests the hypothesis that vasopressin activity, assessed through copeptin levels, is associated with intradialytic hypertension. The primary objective is to evaluate the relationship between copeptin concentrations and blood pressure changes during hemodialysis. Secondary objectives include assessing whether vasopressin's antidiuretic effect is preserved in hemodialysis patients and exploring the contribution of other hormonal pathways involved in fluid and vascular regulation.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
71 (actual)
First submitted
11 Feb 2026
Start date
22 Dec 2025
Primary completion date
1 Mar 2026
Lead sponsor
Central Hospital, Nancy, France
NCT number
NCT07438925

What you commit to

  • Study type: Observational
  • Participants enrolled: 71
  • From 22 Dec 2025 to the primary completion date, 1 Mar 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.

Who the study is looking for

  • Adult patients (≥18 years old).
  • Undergoing chronic hemodialysis treatment \> 3 months.
  • Availability of routine predialysis blood samples for copeptin and biochemical measurements.
  • Availability of blood pressure recordings before, during, and after hemodialysis sessions.
    • No exclusion criteria if inclusion criteria is filled

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. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHRU de Nancy
Coordinator of this site? Confirm its status
Vandœuvre-lès-NancyFranceUnknown status

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