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Incremental Haemodialysis in Incident Patients

Assessment of the Incremental Haemodialysis Security and Effectiveness in Incident Patients

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03239808
Acronym
IHDIP
Enrollment
152
Registered
2017-08-04
Start date
2018-03-14
Completion date
2025-06-30
Last updated
2025-03-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal Disease, End-Stage

Keywords

once-weekly haemodialysis, incremental haemodialysis, randomized clinical trial

Brief summary

Background: Incremental hemodialysis (HD) is a starting regime for renal replacement therapy (RRT) adapted to each patient's necessities. It is mainly conditioned by the residual renal function (RRF). The frequency of sessions with which patients start HD -one or two sessions per week-, is lower than that for conventional HD three times per week. Such frequency is increased (from one to two sessions, and from two to three sessions) as the RRF declines. Methods/Design: IHDIP is a multicenter randomized experimental open trial. It is randomized in a 1:1 ratio and controlled through usual clinical practice, with a low intervention level and non-commercial. It includes 152 patients older than 18 years with chronic renal disease stage 5 and start HD as RRT, with a RRF of ≥ 4ml/min/1.73m2, measured by renal clearance of urea (KrU). The intervention group includes 76 patients who will start with one session of HD per week (incremental HD). The control group includes 76 patients who will start with three sessions per week (conventional HD). The primary purpose is assessing the survival rate, while the secondary purposes are the morbidity rate (hospital admissions), the clinical parameters, the quality of life and the efficiency. Discussion: This study will enable us to know with the highest level of scientific evidence, the number of sessions a patient should receive when starting the HD treatment, depending on his/her RRF.

Detailed description

Conventional thrice-weekly HD for 3 to 5 hours in a health center in an outpatient basis is the most used renal replacement therapy (RRT) regimen (1). However, it has an unacceptable high mortality rate (10%-20% a year). In order to try to improve those results, new regimens have been proposed. They are based on an increase of the HD dose and/or a higher number of sessions (2). Nevertheless, inconsistent results in terms of clinical benefits with such programs have been shown in recently published randomized and controlled trials (3,4), together with a lower rate of vascular access success (5) and a lower maintenance of the RRF (6) The National Kidney Foundation-Kidney Disease Outcomes Quality Initiate (NKD KDOQI 2015)(1) 2015 guidelines allow the reduction in the weekly HD dose for patients with a residual kidney urea clearance (KrU) higher than 3ml/min/1.73m2. In these cases, the renal clearance (Kr) is added to the dialysis clearance (Kd) obtained in 2 sessions per week, thus obtaining the adequate dialysis dose (7,8) Surprisingly enough, few centers follow this recommendation when over 50% of patients start HD with KrU \>3 mL/min (9). Authors like Kalantar-Zadeh et al (9,10) in the U.S.A. or Teruel et al (11) in Spain have published their experience with 2 HD sessions per week in incident patients. Through this regime they have shown that the RRF is preserved and the survival rate is similar to the one obtained with the conventional HD. This is due to the fact that the Kr has much greater clinical weight than Kd7, since the RRF contributes to the production of vitamin D and erythropoietine (12,13), and eliminates the protein-bound uremic toxins that are poorly dialyzed (13,14). In other words, the RRF plays a fundamental role both in the dialysis adequacy and in survival (15,16). Currently, some authors are questioning the number of HD sessions with which a patient should start the renal replacement therapy (RRT) (7, 17-19). Progressive HD is an initiation regimen adapted to the patient's RRF. The frequency increases as the daily diuretic level declines (7, 17-19). The IHDIP trial20 aims at determining whether or not starting with one HD session per week reduces mortality in incident patients and its influence in morbidity (hospital admissions), clinical parameters, quality of life and efficiency with regard to the patients who start RRT with the conventional method.

Interventions

It consists in reducing the frequency or number of sessions per week with which patients start the HD treatment. The experimental group will start with one session/week, then the number of weekly sessions will be increased to two and later to three as per criteria for progression

It is controlled through usual clinical practice, based on starting the HD treatment with three sessions per week (control group).

Sponsors

Hospital Arquitecto Marcide. Ferrol. A Coruña. (Spain)
CollaboratorUNKNOWN
Hospital San Pedro de Alcantara
CollaboratorOTHER
Virgen del Puerto Hospital
CollaboratorOTHER
Hospital Central de la Defensa Gómez Ulla. Madrid (Spain)
CollaboratorUNKNOWN
Hospital Costa del Sol
CollaboratorOTHER
Hospital Obispo Polanco. Teruel (Spain)
CollaboratorUNKNOWN
Hospital de Manises. Valencia (Spain)
CollaboratorUNKNOWN
Hospital Virgen de la Concha. Zamora (Spain)
CollaboratorUNKNOWN
Hospital de Especialidades de las Fuerzas Armadas. Quito (Ecuador)
CollaboratorUNKNOWN
Servicio Extremeño de Salud (Spain)
CollaboratorUNKNOWN
Hospital del SAS de Jerez
CollaboratorOTHER
Hospital Nuestra Sra de Sonsoles. Ávila (Spain)
CollaboratorUNKNOWN
Dialysis Center SM2. Potenza (Italy)
CollaboratorUNKNOWN
Miulli General Hospital
CollaboratorOTHER
Hospital del Rio Hortega
CollaboratorOTHER
Hospital Duran de Buenos Aires
CollaboratorUNKNOWN
Hospital El Bierzo
CollaboratorOTHER
Hospitales Universitarios Virgen del Rocío
CollaboratorOTHER
Hospital Universitario Virgen Macarena
CollaboratorOTHER
University Hospital of Girona Dr. Josep Trueta
CollaboratorNETWORK
Fundación para la Formación e Investigación de los Profesionales de la Salud de Extremadura
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This is a prospective, multicenter, randomized clinical trial. It has two strata: for age (≥or\< 75 years old) and for KrU (≥or\< 5,5 ml/min/1.73m2). It is controlled through usual clinical practice. Intervention consists in reducing the frequency or number of sessions per week with which patients start the HD treatment. The experimental group will start with one session/week, then the number of weekly sessions will be increased to two and later to three as per criteria for progression.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged \>18 years, incident patients with stage 5 CKD who have chosen HD as RRT initiation. * RRF measured by KrU ≥ 4 ml/min/1.73m2. In general, it is advised not to start HD with a KrU\> 7. * Informed consent signed before starting any activity related to the trial.

Exclusion criteria

* Unplanned HD initiation (established in point 7.4 of the protocol) * Non incident patients, in other words, patients who were previously on RRT, either on peritoneal dialysis, or on kidney transplant. * Active neoplasia at the moment of inclusion * Cardiovascular disease defined as: heart failure type IV of the New York Heart Association (NYHA), unstable angina or ischemic cardiopathy which has caused any admission in hospital in the last 3 months. * Cardiorenal syndrome * Active inflammatory disease with immunosuppressive treatment * Hepatorenal syndrome

Design outcomes

Primary

MeasureTime frameDescription
Survival rate24 monthsAssess and compare survival in subjects with one session a week as an RRT starting regimen, compared to those patients who start RRT with the conventional method

Secondary

MeasureTime frameDescription
Residual Kidney Function (RRF) maintenance .24 monthsReduction of glomerular filtration rate (GFR) and tubular function. Average urine volume and percentage of patients with anuria (≤200ml/day in two consecutive measurements).
Analysis of anemia3, 6, 9, 12, 18 and 24 monthsMean hemoglobin levels and Proportion of patients with Hb measurement inside the target range (10.5-12 g/dl) and The erythropoietin resistance index (ERI): ERI = weekly EPO (in UI)/patient's weight (in kg)/Hb (in gr/dl)
Bone-mineral metabolism3, 6, 9, 12, 18 and 24 monthsMean levels of calcium, phosphorus and intac PTH levels. Estimate the percentage of patients within the therapeutic range; Calcium 8,4-9,5mg/dl, Phosphorus 3,5-5,5mg/dl and iPTH 150-300 pg/dl.
Hospital admissions24 monthsNumber of hospitalizations, for any cause; and number of days hospitalized for any cause
Estimation of the effect of treatment on quality of life3, 6, 9, 12, 18 and 24 monthsQuality of life survey values from Kidney Disease and Quality of Life (KDQOL'36 Spanish) will be registered.
Assessing RRT efficiency (costs)12 and 24 monthsThe number of sessions perform in subjects of incremental HDF group Vs number of sessions in the conventional HD group. The cost of each session is defined by the public contest for private haemodialysis clinics arranged by (that work to) the Health Service of Extremadura.
Hypertrophic cardiomyopathy levelsBasal, anual and end of the follow-un visit

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026