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ALdosterone Antagonist Chronic HEModialysis Interventional Survival Trial (ALCHEMIST)

This study is currently recruiting participants.
See Contacts and Locations
Verified May 2017 by University Hospital, Brest
Sponsor:
Collaborators:
Central Hospital, Nancy, France
Institut National de la Santé Et de la Recherche Médicale, France
Information provided by (Responsible Party):
University Hospital, Brest
ClinicalTrials.gov Identifier:
NCT01848639
First received: May 3, 2013
Last updated: May 4, 2017
Last verified: May 2017
May 3, 2013
May 4, 2017
June 2013
June 2023   (Final data collection date for primary outcome measure)
The time to onset of the first incident :non-fatal MI or acute coronary syndrome or hospitalization for heart failure or nonfatal stroke or cardiovascular (CV) death [ Time Frame: 25 months ]
The time to onset of the first incident :non-fatal MI or hospitalization for heart failure or nonfatal stroke or cardiovascular (CV) death [ Time Frame: 25 months ]
Complete list of historical versions of study NCT01848639 on ClinicalTrials.gov Archive Site
  • The cumulate rate of non fatal MI or acute coronary syndrome, hospitalization for heart failure, nonfatal stroke or CV death [ Time Frame: 25 months ]
  • The time to onset of death from i) any cause and ii) from a CV event and iii) from a non CV cause [ Time Frame: 25 months ]
  • The time of survival without a major CV event (non fatal MI, acute coronary syndrome, hospitalization for heart failure, non-fatal stroke, cardiac arrest resuscitation) [ Time Frame: 25 months ]
  • Incidence of procedures related to stenosis or vascular access thrombosis for hemodialysis (HD) [ Time Frame: 25 months ]
  • Incidence of coronary or peripheral revascularizations (including lower limb amputations) [ Time Frame: 25 months ]
  • Blood pressure and its inter visit variability [ Time Frame: 25 months ]
  • The occurrence of atrial fibrillation [ Time Frame: 25 months ]
  • Incidence of hyperkalemia> 6 mmol/l [ Time Frame: 25 months ]
  • Estimation of the effect of treatment on quality of life. [ Time Frame: 25 months ]
  • The cumulate rate of nonfatal MI, hospitalization for heart failure, nonfatal stroke or CV death [ Time Frame: 25 months ]
  • The time to onset of death from i) any cause and ii) from a CV event and iii) from a non CV cause [ Time Frame: 25 months ]
  • The time of survival without a major CV event (nonfatal MI, hospitalization for heart failure, non-fatal stroke, cardiac arrest resuscitation) [ Time Frame: 25 months ]
  • Incidence of procedures related to stenosis or vascular access thrombosis for hemodialysis (HD) [ Time Frame: 25 months ]
  • Incidence of coronary or peripheral revascularizations (including lower limb amputations) [ Time Frame: 25 months ]
  • Blood pressure and its inter visit variability [ Time Frame: 25 months ]
  • The occurrence of atrial fibrillation [ Time Frame: 25 months ]
  • Incidence of hyperkalemia> 6 mmol/l [ Time Frame: 25 months ]
  • Estimation of the effect of treatment on quality of life. [ Time Frame: 25 months ]
  • Ancillary study:establishment of a biological collection (serum bank and DNA biobank) for future biomarker studies [ Time Frame: 25 months ]
  • Ancillary study:morbimortality data [ Time Frame: 3, 5 and 10 years of follow-up after the double-blind study ]
Same as current
 
ALdosterone Antagonist Chronic HEModialysis Interventional Survival Trial
ALdosterone Antagonist Chronic HEModialysis Interventional Survival Trial (ALCHEMIST), Phase III b
This study is designed to etablish the effects of spironolactone in comparison to placebo on the composite endpoint of nonfatal Myocardial Infarction (MI) and acute coronary syndrome, hospitalization for heart failure, nonfatal stroke or cardiovascular-induced death. The primary endpoint will be the time to onset of the first incident.
  • During a run-in period : Spironolactone will be initially administered per os at a 25 mg dose per two days in practice after the session, three times per week
  • Patients will be randomized (spironolactone vs. placebo) and titrated over one month to a maximum single dose of 25 mg/d
  • However if kalemia is greater than or equal to 5.5 mmol / l twice on this run-in period or on the day of randomization, patient won't be randomized.
  • A pre-specified algorithm for the management of the risk of incident hyperkalemia will be followed, including dose adjustment, temporary cessation of study treatment, in addition to usual dietary measures and the use of chelating resins and low-potassium dialysis baths
  • Patients will be followed for a mean of 2 years.
Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Participant, Care Provider, Investigator
Primary Purpose: Treatment
End Stage Renal Failure on Dialysis
  • Drug: Spironolactone
    After a month in run-in period under 25 mg per 2 days of spironolactone administered per os in practice after dialysis session three times a week, patients will be randomized to spironolactone. The dose should be increased to 25 mg once daily and could be adjusted in using an algorithm used in the EPHESUS and EMPHASIS-HF trials.
  • Drug: Placebo
    After a month in run-in period under 25 mg per 2 days of spironolactone administered per os in practice after dialysis session three times a week, patients will be randomized to placebo. The dose should be increased to 25 mg once daily and could be adjusted in using an algorithm used in the EPHESUS and EMPHASIS-HF trials.
  • Active Comparator: Spironolactone
    After a month in run-in period under 25 mg per 2 days of spironolactone administered per os in practice after dialysis session three times a week, patients will be randomized to spironolactone. The dose should be increased to 25 mg once daily and could be adjusted in using an algorithm used in the EPHESUS and EMPHASIS-HF trials.
    Intervention: Drug: Spironolactone
  • Placebo Comparator: Placebo
    After a month in run-in period under 25 mg per 2 days of spironolactone administered per os in practice after dialysis session three times a week, patients will be randomized to placebo. The dose should be increased to 25 mg once daily and could be adjusted in using an algorithm used in the EPHESUS and EMPHASIS-HF trials.
    Intervention: Drug: Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
825
June 2024
June 2023   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Written informed consent
  • Health insurance beneficiary
  • Men and women, on hemodialysis for at least 45 days for end-stage renal disease regardless of the aetiology including diabetes, with at least 3 hemodialysis sessions per week AND presenting at least one of following comorbidities or CV risk factors:
  • left ventricular mass > 130 g/m2 in men and 100 g/m2 in women measured during the twelve months preceding inclusion
  • left ventricular ejection fraction < 40% measured during the twelve months preceding inclusion
  • diabetes
  • history of Cardiovascular disease: coronary artery disease, symptomatic lower limb peripheral arterial disease, carotid or renal artery stenosis > 50%, stroke, hospitalization for heart failure or CRP> 5 mg / l for 3 months without infectious or neoplastic disease documented in progress

Exclusion Criteria:

  • history of hypersensitivity to spironolactone or galactose intolerance
  • the Lapp lactase deficiency or malabsorption of glucose or galactose
  • hyperkalemia > 5.5 mmol/l during the two weeks prior to enrolment
  • history of unscheduled hemodialysis for hyperkalemia during the last six months
  • hospitalization for hyperkalemia during the last six months
  • patients with imperative indication of a combination of ACEI and sartan or renin inhibitor (each being authorized separately), NSAIDS, Cox-2 inhibitors
  • kidney transplant scheduled within the year
  • symptomatic interdialytic hypotension
  • acute systemic disease
  • uncompensated hypothyroidism
  • acute hyperthyroidism
  • any prior or concomitant clinical condition compromising the inclusion, in the discretion of the investigator
  • cardiac transplant
  • severe uncontrolled arrhythmia
  • stroke within 3 months prior to enrolment
  • acute coronary syndrome in the previous month inclusion
  • recent (1 month) or planned coronary revascularization by angioplasty
  • recent (3 months) or planned cardiovascular surgery (excluding HD vascular access)
  • non menopausal women or without effective contraceptive methods
  • pregnancy, breastfeeding or planning a pregnancy within 2 years
  • non compliance
  • protected adult
  • SBP > 200 mmHg and/or DBP > 110 mmHg
  • Concomitant treatment can not be stopped by another potassium-sparing diuretic, a potassium supplements, AINS or Cox 2 inhibitors
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact: Patrick ROSSIGNOL, Pr +33383157320 p.rossignol@chu-nancy.fr
Belgium,   France,   Guadeloupe,   Monaco,   Switzerland
Martinique
 
NCT01848639
ALCHEMIST
RB 12-079 ( Other Identifier: CHRU Brest )
Yes
Not Provided
Not Provided
Not Provided
University Hospital, Brest
University Hospital, Brest
  • Central Hospital, Nancy, France
  • Institut National de la Santé Et de la Recherche Médicale, France
Not Provided
University Hospital, Brest
May 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP