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Incremental Haemodialysis in Incident Patients (IHDIP)

Primary Purpose

Renal Disease, End-Stage

Status
Active
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Incremental haemodialysis
Conventional haemodialysis
Sponsored by
Fundación para la Formación e Investigación de los Profesionales de la Salud de Extremadura
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Disease, End-Stage focused on measuring once-weekly haemodialysis, incremental haemodialysis, randomized clinical trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • FundeSalud. Junta de Extremadura
  • Hospital Virgen del Puerto
  • Hospital San Pedro de Alcántara

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group

Control group

Arm Description

76 patients who start RRT with the incremental HD regimen.

76 patients who start RRT with the conventional HD (3 sessions per week)

Outcomes

Primary Outcome Measures

Survival rate
Assess 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 Outcome Measures

Hospital admissions
Number of hospitalizations, for any cause; and number of days hospitalized for any cause
Residual Kidney Function (RRF) maintenance .
Reduction 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 anemia
Mean 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 metabolism
Mean 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.
Hypertrophic cardiomyopathy levels
Estimation of the effect of treatment on quality of life
Quality of life survey values from Kidney Disease and Quality of Life (KDQOL'36 Spanish) will be registered.
Assessing RRT efficiency (costs)
The 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.

Full Information

First Posted
July 4, 2017
Last Updated
February 19, 2023
Sponsor
Fundación para la Formación e Investigación de los Profesionales de la Salud de Extremadura
Collaborators
Hospital Arquitecto Marcide. Ferrol. A Coruña. (Spain), Hospital San Pedro de Alcantara, Virgen del Puerto Hospital, Hospital Central de la Defensa Gómez Ulla. Madrid (Spain), Hospital Costa del Sol, Hospital Obispo Polanco. Teruel (Spain), Hospital de Manises. Valencia (Spain), Hospital Virgen de la Concha. Zamora (Spain), Hospital de Especialidades de las Fuerzas Armadas. Quito (Ecuador), Servicio Extremeño de Salud (Spain), Hospital del SAS de Jerez, Hospital Nuestra Sra de Sonsoles. Ávila (Spain), Dialysis Center SM2. Potenza (Italy), Miulli General Hospital, Hospital del Río Hortega, Hospital Duran de Buenos Aires, Hospital El Bierzo, Hospitales Universitarios Virgen del Rocío, Hospital Universitario Virgen Macarena, Hospital Universitario Dr J Trueta
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1. Study Identification

Unique Protocol Identification Number
NCT03239808
Brief Title
Incremental Haemodialysis in Incident Patients
Acronym
IHDIP
Official Title
Assessment of the Incremental Haemodialysis Security and Effectiveness in Incident Patients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 14, 2018 (Actual)
Primary Completion Date
June 6, 2024 (Anticipated)
Study Completion Date
September 6, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundación para la Formación e Investigación de los Profesionales de la Salud de Extremadura
Collaborators
Hospital Arquitecto Marcide. Ferrol. A Coruña. (Spain), Hospital San Pedro de Alcantara, Virgen del Puerto Hospital, Hospital Central de la Defensa Gómez Ulla. Madrid (Spain), Hospital Costa del Sol, Hospital Obispo Polanco. Teruel (Spain), Hospital de Manises. Valencia (Spain), Hospital Virgen de la Concha. Zamora (Spain), Hospital de Especialidades de las Fuerzas Armadas. Quito (Ecuador), Servicio Extremeño de Salud (Spain), Hospital del SAS de Jerez, Hospital Nuestra Sra de Sonsoles. Ávila (Spain), Dialysis Center SM2. Potenza (Italy), Miulli General Hospital, Hospital del Río Hortega, Hospital Duran de Buenos Aires, Hospital El Bierzo, Hospitales Universitarios Virgen del Rocío, Hospital Universitario Virgen Macarena, Hospital Universitario Dr J Trueta

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Disease, End-Stage
Keywords
once-weekly haemodialysis, incremental haemodialysis, randomized clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
152 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
76 patients who start RRT with the incremental HD regimen.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
76 patients who start RRT with the conventional HD (3 sessions per week)
Intervention Type
Procedure
Intervention Name(s)
Incremental haemodialysis
Intervention Description
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
Intervention Type
Procedure
Intervention Name(s)
Conventional haemodialysis
Intervention Description
It is controlled through usual clinical practice, based on starting the HD treatment with three sessions per week (control group).
Primary Outcome Measure Information:
Title
Survival rate
Description
Assess 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
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Hospital admissions
Description
Number of hospitalizations, for any cause; and number of days hospitalized for any cause
Time Frame
24 months
Title
Residual Kidney Function (RRF) maintenance .
Description
Reduction of glomerular filtration rate (GFR) and tubular function. Average urine volume and percentage of patients with anuria (≤200ml/day in two consecutive measurements).
Time Frame
24 months
Title
Analysis of anemia
Description
Mean 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)
Time Frame
3, 6, 9, 12, 18 and 24 months
Title
Bone-mineral metabolism
Description
Mean 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.
Time Frame
3, 6, 9, 12, 18 and 24 months
Title
Hypertrophic cardiomyopathy levels
Time Frame
Basal, anual and end of the follow-un visit
Title
Estimation of the effect of treatment on quality of life
Description
Quality of life survey values from Kidney Disease and Quality of Life (KDQOL'36 Spanish) will be registered.
Time Frame
3, 6, 9, 12, 18 and 24 months
Title
Assessing RRT efficiency (costs)
Description
The 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.
Time Frame
12 and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Javier L Deira Lorenzo, PhD MD
Organizational Affiliation
Servicio Extremeño de Salud
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Miguel A Suarez Santisteban, MD
Organizational Affiliation
Servicio Extremeño de Salud
Official's Role
Principal Investigator
Facility Information:
Facility Name
FundeSalud. Junta de Extremadura
City
Mérida
State/Province
Badajoz
ZIP/Postal Code
06800
Country
Spain
Facility Name
Hospital Virgen del Puerto
City
Plasencia
State/Province
Cáceres
ZIP/Postal Code
10600
Country
Spain
Facility Name
Hospital San Pedro de Alcántara
City
Cáceres
ZIP/Postal Code
10003
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Yes
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Incremental Haemodialysis in Incident Patients

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