- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00307463
Effects of Strict Volume Control in Hypertensive Hemodialysis Patients on Cardiac Structure and Chronic Inflammation
Effects of Strict Volume Control in Hypertensive Hemodialysis Patients on Cardiac Structure and Chronic Inflammation: a Randomised, Prospective and Controlled Study
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This randomised, controlled and prospective study aims mainly to investigate the effects of two approaches to control blood pressure in hypertensive hemodialysis patients; using antihypertensive drugs versus persistent strict volume control without using antihypertensive drugs on cardiac structure (mainly left ventricular hypertrophy)and inflammation.
We hypothesize that better blood pressure control and regression of left ventricular mass may be reached by a policy of strict volume control consisting of strict dietary salt restriction and persistent ultrafiltration.
258 Hypertensive hemodialysis patients (BP>130/80 mmHg and/or being on antihypertensive medication) will be randomized to two arms:
Group 1: Antihypertensive medicine will be stopped and strict volume control policy will be applied.
Group 2: Antihypertensive medicine will be continued. Target BP will be 130/80 mmHg in both groups.
The patients will be evaluated at 12 months for primary outcomes. Primary end-points are significant changes in left ventricular hypertrophy and left ventricular mass and significant change in left ventricular end-diastolic volume.
Secondary end-points are changes in post-dialysis weight, changes in hematocrit, albumin, BNP and hsCRP levels.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
-
-
-
Adana, Kalkun, 01100
- Adana Numune Research and Education Hospital
-
-
Izmir
-
Bornova, Izmir, Kalkun, 35100
- Ege University School of Medicine Division of Nephrology
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- aged between 18-70 years old
- on maintenance bicarbonate hemodialysis scheduled thrice weekly, at least 12 hours/week
- willingness to participate in the study with a written informed consent.
Exclusion Criteria:
- to be scheduled for living donor renal transplantation
- to have serious life-limiting co-morbid situations; namely active malignancy, active infection, end-stage cardiac, pulmonary, or hepatic disease; pregnancy or lactating
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Aktiv komparator: strict volume control policy
strict volume control policy: Antihypertensive medicine will be stopped and strict volume control policy will be applied.
|
strict volume control by UF and dietary salt restriction
|
Andet: antihypertensive drugs administration
antihypertensive drugs administration: Antihypertensive medicine will be continued.
Target BP will be 130/80 mmHg in both groups.
|
continue antihypertensive medications
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
regression of left ventricular hypertrophy
Tidsramme: one year
|
one year
|
regression of left ventricular mass
Tidsramme: one year
|
one year
|
change in left ventricular end-diastolic volume
Tidsramme: one year
|
one year
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
change in post-dialysis weight, changes in hematocrit, albumin, changes in BNP and hsCRP levels
Tidsramme: one year
|
one year
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Studiestol: Ercan Ok, M.D, Ege University School of Medicine Nephrology Department
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Ege1336
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Slutstadie nyresygdom
-
Universitaire Ziekenhuizen KU LeuvenAfsluttetForekomst af Augmented Renal Clearance | Risikofaktorer for øget renal clearanceBelgien
-
Medical University of ViennaAfsluttetGlomerulær filtreringshastighed | Fedtsyrer, ikke-esterificerede | Renal Cirkulation | Renal Plasma FlowØstrig
-
The First People's Hospital of ChangzhouIkke rekrutterer endnu
-
Andrew B AdamsBristol-Myers SquibbAfsluttet
-
Hospices Civils de LyonAfsluttetSkadelig virkning | Renal toksicitetFrankrig
-
University Health Network, TorontoAfsluttetGlomerulær filtreringshastighed | Renal blodgennemstrømningCanada
-
National Cancer Institute (NCI)AfsluttetLunge | Bryst | Ovarie | Cervikal | RenalForenede Stater
-
Oregon Health and Science UniversityAfsluttet- Undersøgelsesfokus: Renal retention af lipidmikroboblerForenede Stater
-
Assiut UniversityIkke rekrutterer endnuLevertransplantation; Komplikationer | Renal komplikation af proceduren