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AnaemiaPhase 4NCT00396435

Correction of Anaemia and Progression of Renal Failure on Transplanted Patients

A Phase 4 study testing Neorecormon in people with Anaemia and Renal Transplantation, run by Centre Hospitalier Universitaire, Amiens at 20 sites in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to evaluate, on renal transplanted patients with CGD, the effect of two levels of haemoglobin on quality of life at 6 months and the speed of progression of renal function degradation at 24 months. This study will recruit 140 patients in 21 centers in France. Read more about this study

Who is it for?
Ages 18 to 70 years
Conditions the study is for
Anaemia, Renal Transplantation, Kidney Failure
What is being tested?
Neorecormon
Could I receive a placebo?
No, everyone receives an active treatment
How many people
128 participants
Where
20 sitesFrance
Study dates
Apr 2004to May 2010
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Adults male or female of 18 years male or female sex to 70 years
  • Patients having profited from one 1st or one the 2nd transplantation
  • Patients transplanted since more than 1 year and less than 20 years.
  • Patients having a CDG defined by a clearance of creatinin, lower than 50 ml/mn/1,73 m2 (according to Gault and Cockcroft) and whose renal function is stable over the last 3 months (variation of Scr of less than 20% over the last 3 months)
  • Patients presenting an anaemia: Hb lower than 11.5 g/dl
  • No deficiency out of iron: Saturation of the transferrin > 20% and ironnemia > 50 mg/l at the time of the screening visit
  • Patients having given their written consent

Who cannot join

  • Major forms of drepanocytosis or thalassaemia
  • Iron Deficit (CST < 20% or ferritin < 50 mg/l)
  • Haemolysis (haptoglobin < 0,30 g/l)
  • Severe renal insufficiency: Clcr < 20 ml/min/1,73 m2
  • Severe Hyperparathyroidy (serum PTH > 800 pg/ml)
  • Evolutionary chronic inflammatory Disease (CRP > 15 mg/l)
Show all 25Show fewer
  • Acute or chronic infectious disease
  • Evolutionary neoplasic Disease
  • Infection by the HIV and viral cirrhosis
  • Recent Antecedents of MI or AIT (< 3 months)
  • Severe Arteritis of the lower limbs (Stage III or IV)
  • Acute Rejection requiring a treatment in the 3 previous months
  • Blood Transfusion on the last 3 months
  • Evolutionary GI Ulcer on the last 3 months
  • Severe Arterial HyperTension not controlled by medicamentous treatment (NOT > 170 mm Hg or PAD > 100 mm Hg under treatment)
  • Epilepsy of recent diagnosis
  • Relevant biological value(at screening visit) : - Proteinuria > 3 g/24h
  • Serum Albumin < 30 g/l
  • Platelets > 600.000/µl
  • Programmed heavy surgery
  • Pregnancy or breast feeding
  • Administration of an experimental drug in the 30 days preceding the screening visit
  • Known Over-sensitiveness to Epoetin beta
  • Patients under Sirolimus
  • Patients under EPO at screening visit

Trial locations and contacts

20 sites in 1 country.

20 sites in 1 country

France20 sites
  • Hôpital Sud

    Amiens, 80000

  • Hôpital de Bois Guillaume

    Bois-Guillaume, 76230

  • Hôpital Pellegrin

    Bordeaux, 33076

  • Hôpital Clémenceau

    Caen, 14033

  • CHU Clermont Ferrand - Hôpital Gabriel Monpied

    Clermont-Ferrand, 63003

  • Hôpital Henri Mondor

    Créteil, 94010

  • Hôpital de la Tronche

    Grenoble, 38043

  • Hôpital Calmette

    Lille, 59037

  • Hôpital Dupuytren

    Limoges, 87052

  • Hôpital de la Conception

    Marseille, 13385

  • Hôpital Pasteur

    Nice, 06002

  • Hôpital Necker - Enfants Malades

    Paris, 75743

  • Hôpital de la Milétrie

    Poitiers, 86021

  • Hôpital Maison Blanche

    Reims, 51092

  • Hôpital Pontchaillou

    Rennes, 35033

  • Hôpital Civil

    Strasbourg, 67091

  • Hôpital Foch

    Suresnes, 92151

  • Hôpital Rangueil

    Toulouse, 33076

  • CHU de Tours - Hôpital Bretonneau

    Tours, 37044

  • Hôpital Brabois

    Vandœuvre-lès-Nancy, 54500

Other trials in France

About this study

Official title: Multicenter, Prospective, Randomised, Open-label Study, Evaluating the Effect of Two Levels of Haemoglobin on Quality of Life and Speed of Progression of Renal Insufficiency on Renal Transplanted Patients With Chronic Graft Dysfunction (CGD)

The purpose of this study is to evaluate, on renal transplanted patients with CGD, the effect of two levels of haemoglobin on quality of life at 6 months and the speed of progression of renal function degradation at 24 months.

This study will recruit 140 patients in 21 centers in France.

Read the detailed description

The number of patients arriving each year at the stage of final renal insufficiency (IRT) and requiring the dialysis of substitution does not cease growing, in parallel with continuous ageing of the population in industrialized countries. The incidence of the IRT is approximately 110 new patients per million inhabitants per year, which represents an annual progression from approximately 4% to 8% according to areas.Approximately 35000 patients are currently treated by dialysis, 90% by hemodialysis and 10% per peritoneal dialysis . The other alternative to the treatment of the IRT is renal transplantation. Approximately 2000 patients are transplanted each year in France, and it is estimated that a minimum of 3000 transplantations should annually be carried out in order to answer at the request of the patients registers on a chronic program of dialysis and in to be transplanted age.

The total number of patients living with a functional graft is approximately 15000.

The IRT is a major problem of public health and its cost is considerable: for less than 50000 patients, this one represents nearly 4% of the annual budget of the social security. To slow down the progression of the IRC represents a major therapeutic challenge, including at the transplanted patients.

The physiopathological mechanisms proposed to explain the harmful role of anaemia in the progression of the renal lesions during the IRC rest on the tissue hypoxia induced by the reduction in haemoglobin. The tissue hypoxia supports the development of the interstitial fibrosis by stimulating the production of type I collagen and some inhibitors of metalloproteases, implied in the extracellular matrix degradation. The hypoxia also stimulates the synthesis of TGF-beta, pro-fibrosing factors implied in the progression of many renal diseases, in particular the nephropathy diabetic. By reducing the hypoxia thanks to the correction of anaemia by the EPO, one can hope to slow down the progression of the interstitial fibrosis, and thus the progression of the renal insufficiency. Lastly, the correction of anaemia reduces resistance to insulin and the secondary hyperinsulinism to uraemia, improves the dyslipidemia and the oxidizing stress, factors also implied in the progression of many nephropathies, diabetic or not.

It appears that anaemia is a factor of risk of progression of the chronic nephropathies. To slow down the progression of the chronic dysfunction of the graft is an important challenge because of shortage of graft and impossibility, in the current state of the French centers of renal transplantation to carry out the number of necessary grafts to provide for the current waiting list. Our hypothesis, if it is checked, should make it possible to very appreciably improve the quality of life of the transplanted patients and to slow down the progression of their IRC, thus delaying the duration before return in dialysis.

Population: Renal patients transplanted since at least 12 months, presenting a CGD defined by 20 ml/mn/1,73 m2 > Clcr < 50 ml/mn/1,73 m2 and an anaemia (Hb < 11,5 g/dl)

The patients answering the criteria of selection will be assigned by randomization with the one of the two following groups:

  • Group a: target haemoglobin: 13 to 15 g/dl
  • Group b: target haemoglobin: 10,5 to 11,5 g/dl

Criteria of inclusion

  • Adults of male or female sex of more than 18 years
  • Patients having profited from one 1st or one the 2nd renal Transplantation
  • Patients Transplanted since more than 1 year
  • Patients having a CGD defined by Clcr < 50 ml/mn/1,73 m2
  • Patients presenting an anaemia: Hb lower than 11,5 g/dl
  • Absence of deficiency out of iron
  • Patients having given their in writing consent

Study Treatment: Neorecormon® (Epoétine beta) under cutaneous injection

The objective of the study is to show a difference between group A "haemoglobin target: 13 to 15 g/dl" and group it B "haemoglobin target: 10,5 to 11,5 g/dl", with regard to the renal function.

The calculation of the number of patients is thus based on a model of covariance analysis in repeated measurements of clearance of creatinin on the whole of the times evaluated between J0 and M24 and on the following hypothesis:

  • H0: no effect groups during the two years of follow-up
  • H1: Effect groups, evolution different from the values of Clcr during the follow-up

The alfa-risk (probability of rejecting H0 wrongly) was fixed at 5% The beta-risk (probability of keeping H0 wrongly) at 10% The total number of patients to be randomized was estimated at 140 (70 by group) This number of patients will also make it possible to test the scores of quality of life with a power higher than 90%

Being tested
Neorecormon
Keywords
anaemia, renal transplantation, kidney failure
Medical subject headings
Anemia, Renal Insufficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • NeorecormonDrug

    Also called Epoetin

    Administration SC one a week in patients randomized in group A Administration SC if Hb below 10.5 g/dl in group B

Study groups in NCT00396435
Study groupRoleWhat they receive
Group AExperimentalHigh Hb target
Receives: Drug: Neorecormon
Group BActive comparatorLow Hb Target
Receives: Drug: Neorecormon

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. eClcr by Cockcroft formula

    Measured: 2 years

Secondary outcomes (9)
  1. Measure CDG by the clearance of Iohexol

    Measured: 2 years

  2. 1/Scr at J0, 6 months, 12 months, 18 months and 24 months Scr with J0, 6, 12, 18 and 24 months

    Measured: 2 years

  3. Proteinuria and micro-albuminuria at J0, 12 and 24 months

    Measured: 2 years

  4. Evaluation of the quality of life in the 2 groups of patients per self-evaluation at J0 and 6 months

    Measured: 6 months

  5. Adverse events, in particular cardiovascular events: MI, AIT, Arteritis of lower limb, revascularisation,

    Measured: 2 years

  6. Biological tolerance: Albuminemia, pre-albuminemia, CRP, plasmatic Cholesterol, HDL and LDL

    Measured: 2 years

  7. Level of blood pressure at the beginning and the end of the study and comparison of the number of antihypertensive drugs received by patients before and after the 24 months of follow-up

    Measured: 2 years

  8. Number of units of beta-EPO managed in the 2 groups

    Measured: 2 years

  9. Number of patients receiving blood transfusions

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted7 Nov 2006 (estimated)
  2. Study startApr 2004
  3. Primary completionApr 2009
  4. Study completionMay 2010

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
128 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00396435
Sponsor's protocol ID
CAPRIT
Status last verified
Sep 2025
First submitted
3 Nov 2006
Last updated
23 Sep 2025
Results posted
No
Data monitoring committee
No

Publications

  • Choukroun G, Kamar N, Dussol B, Etienne I, Cassuto-Viguier E, Toupance O, Glowacki F, Moulin B, Lebranchu Y, Touchard G, Jaureguy M, Pallet N, Le Meur Y, Rostaing L, Martinez F; CAPRIT study Investigators. Correction of postkidney transplant anemia reduces progression of allograft nephropathy. J Am Soc Nephrol. 2012 Feb;23(2):360-8. doi: 10.1681/ASN.2011060546. Epub 2011 Dec 22.

    PubMed 22193388
  • Chung EY, Palmer SC, Saglimbene VM, Craig JC, Tonelli M, Strippoli GF. Erythropoiesis-stimulating agents for anaemia in adults with chronic kidney disease: a network meta-analysis. Cochrane Database Syst Rev. 2023 Feb 13;2(2):CD010590. doi: 10.1002/14651858.CD010590.pub3.

    PubMed 36791280

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Neorecormon in people with Anaemia and Renal Transplantation, run by Centre Hospitalier Universitaire, Amiens at 20 sites in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 25 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 20 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

eClcr by Cockcroft formula (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00396435, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Sep 2025.

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