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Prospective Observational Multicenter Study of Patients With AH and CKD Markers in Kazakhstan (PROGRESS-CKD)
Prospective Observational Multicenter Study of Patients With AH and CKD Markers in Kazakhstan (PROGRESS-CKD)

NCT06744335

Active Not RecruitingN/A

Sponsor: AstraZeneca

Conditions: Rate of CKD Diagnosis in Patients With AH and CKD Markers, Demographic and Clinical Characteristics for Those Patients, Routine Therapy Before and After the Diagnosis of CKD

Countries: Kazakhstan

Multicenter, non-interventional PRospective Observational study with retrospective analysis to describe the rate of CKD diaGnosis in patients with aRtErial hypErtenSion and CKD markerS in Kazakhstan

Eligibility overview

Sex: ALL

Age: 18 Years to

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria
Inclusion Criteria:

Age ≥18 years at the time of inclusion;

* Patient signed and dated written informed consent form (ICF) in accordance with ICH GCP and local legislation prior to inclusion in the study for the prospective observational cohort;
* Established diagnosis of hypertension, diagnosed in accordance with current clinical guidelines for hypertension, i.e. in adults, i.e. systolic blood pressure (SBP) ≥140 mmHg and/or diastolic blood pressure (DBP) ≥90 mmHg. when measured at two different visits
* Laboratory markers of CKD (eGFR \<60 mL/min/1.73 m2 and/or albuminuria/proteinuria\*) measured during the period ≤12 months prior to inclusion in the study and persisting ≥3 months between two measurements without a recorded diagnosis of CKD in the primary medical record prior to inclusion;

  \* any of the following: urine albumin/creatinine ratio (UACR) ≥30 mg/g (3 mg/mmol), Urine protein-creatinine ratio (uPCR) ≥150 mg/g (15 mg/mmol), albuminuria ≥30 mg/d or Urine protein-creatinine ratio (uPCR) ≥0.15 mg/d.
* Absence of documented diagnosis of CKD in the patient's medical records prior to inclusion in the study

Exclusion Criteria:

* Absence of a signed ICF in patients in the prospective follow-up group

  * Participation in any randomized controlled trial within 3 months prior to inclusion in this study or during participation in this study
  * An established diagnosis of type 1 or type 2 diabetes mellitus.
  * Diagnosis of symptomatic chronic heart failure (CHF), NYHA functional class III-IV, documented in the patient's medical records
  * Diagnosis of AH of secondary genesis
Locations (28)
  • Temirlanovka, Turkistan Oblast, Kazakhstan
  • Aktobe, Kazakhstan
  • Almaty, Kazakhstan
  • Almaty, Kazakhstan
  • Almaty, Kazakhstan
  • Almaty, Kazakhstan
  • Almaty, Kazakhstan
  • Almaty, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Astana, Kazakhstan
  • Esik, Kazakhstan
  • Karaganda, Kazakhstan
  • Karaganda, Kazakhstan
  • Kostanay, Kazakhstan
  • Semey, Kazakhstan
  • Shymkent, Kazakhstan
  • Shymkent, Kazakhstan
  • Stepnogorsk, Kazakhstan
  • Turkestan, Kazakhstan
  • Uzynaghash, Kazakhstan