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Non-Dialysis Dependent Severe Renal DysfunctionPhase 3SeRenaD-CPBNCT00720967

Preop Hemodialysis or Intraop Ultrafiltration for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery

A Phase 3 study testing Open Heart Surgery (OHS), Intraoperative Modified Ultrafiltration (MUF) and Hemodialysis (HD) in people with Non-Dialysis Dependent Severe Renal Dysfunction and Cardiovascular Disease, run by University Hospital, Geneva at 7 sites in 5 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

The purpose of this study is to determine whether preoperative hemodialysis or intraoperative modified ultrafiltration are effective for patients with non-dialysis dependent severe renal dysfunction undergoing open heart surgery. Read more about this study

Who is it for?
Ages 18 to 95 years
What is being tested?
Open Heart Surgery (OHS), Intraoperative Modified Ultrafiltration (MUF) and Hemodialysis (HD)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
450 participants
Where
7 sitesin 5 countries
Study dates
Nov 2008to Nov 2012
Phase
Phase 3
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 95 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18 years or older
  • Diagnosis of SCr > 180 µmol/L or 2.0 mg/dL, and/or a GFR < 30 mL/min/1.73 m2.
  • Indication for elective open heart surgery under CPB.

Who cannot join

  • History of chronic or recent HD.
  • Emergency status.
  • Off-pump surgery.
  • Failure to obtain patient consent documented by a signed consent form.

Trial locations and contacts

7 sites in 5 countries.

Erman Pektok, MD contact

+41.76.3169990

epektok@hotmail.com

Patrick O. Myers, MD contact

+41.22.3727630

patrick.myers@hcuge.ch

7 sites in 5 countries

Turkey (Türkiye)3 sites
  • Ankara University, Department of Cardiovascular Surgery

    Ankara, 06340

    Ruchan Akar, MD, +90.312.5082202, akarruchan@gmail.com

    Ruchan Akar, MD

  • Pamukkale University, Department of Cardiovascular Surgery

    Denizli, 20070

    Gokhan Onem, MD, +90.258.4440728 ext. 2294, gonem@pau.edu.tr

    Gokhan Onem, MD

  • Gaziantep University, Department of Cardiovascular Surgery

    Gaziantep, 27310

    Hasim Ustunsoy, MD, +90.342.3603910, hustunsoy@yahoo.com

    Hasim Ustunsoy, MD

Other trials in Turkey (Türkiye)

France1 site
  • University of Lyon, Hopital Cardiothoracique Louis Pradel

    Lyon

    Jean-Francois I. Obadia, MD, PhD, +33.4.75357546, jean-francois.obadia@chu-lyon.fr

    Jean-Francois I. Obadia, MD, PhD

Other trials in France

Germany1 site
  • German Heart Institute Berlin

    Berlin, D-13353

    Roland Hetzer, MD, +49.30.45932000, hetzer@dhzb.de

    Roland Hezter, MD

Other trials in Germany

Spain1 site
  • Hospital Clinico, University of Barcelona, Department of Cardiovascular Surgery

    Barcelona

    Carlos A. Mestres, MD, PhD, +34.93.2275515, cmestres@clinic.ub.es

    Carlos A. Mestres, MD, PhD

Other trials in Spain

Switzerland1 site
  • University Hospital of Geneva, Service for Cardiovascular Surgery

    Geneva, 1211

    Erman Pektok, MD, +41.76.3169990, epektok@hotmail.com

    Patrick O. Myers, MD, +41.22.3727630, patrick.myers@hcuge.ch

Other trials in Switzerland

About this study

Official title: Influence of Preoperative Hemodialysis or Intraoperative Modified Ultrafiltration on Postoperative Outcome for Patients With Severe Renal Dysfunction Undergoing Open Heart Surgery: Randomized, Controlled, Multicenter Clinical Trial

The purpose of this study is to determine whether preoperative hemodialysis or intraoperative modified ultrafiltration are effective for patients with non-dialysis dependent severe renal dysfunction undergoing open heart surgery.

Read the detailed description
  1. BACKGROUND

1.1. RENAL DYSFUNCTION AND OPEN HEART SURGERY:

The incidences of both cardiovascular disease (CVD) and chronic renal dysfunction (RD) are increasing with the aging population in the western world (1). The intense relationship between the pathogenesis of CVD and chronic RD has recently been reviewed by Schiffrin et al, in detail (2). They both have common risk factors such as diabetes, hypertension, activation of renin-angiotensin system, endothelial dysfunction, oxydative stress, etc. Besides, each has an impact on the other's outcome. On the one hand, CVD is the most frequent cause of death in chronic RD patients (3). On the other hand, even mild chronic RD is one of the major risk factors of postoperative mortality and morbidity after cardiac operations (4, 5). The mechanism is not clear yet, however, volume overload, electrolyte imbalance and inflammatory state created by cardiopulmonary bypass (CPB) may have an impact. Zakeri et al showed that in-hospital mortality after isolated primary coronary artery bypass grafting (CABG) increases exponentially with increasing levels of renal dysfunction (6). They reported an in-hospital mortality of 2.2%, 4.3%, 9.3% and 14.8% in patients who have a preoperative serum creatinine level (SCr) of <130 µmol/L, 130-149 µmol/L, 150-179 µmol/L and 180-199 µmol/L, respectively. These results were similar to the study published previously by Weerasinghe et al with the same cut-off levels of SCr (7). Using the Glomerular Filtration Rate (GFR) instead of SCr, Cooper et al. came to the same conclusion after analysing 483,914 patients receiving isolated CABG in the Society of Thoracic Surgeons (STS) National Adult Cardiac Database (5). They reported that operative mortality rose inversely with declining renal function, from 1.3% for those with normal renal function to 1.8%, 4.3% and 9.3% for patients with mild, moderate and severe RD, respectively. Another study regarding the effect of preoperative RD on mortality after valve surgery was also published with a relatively smaller patient population (8). Although the RD group had significantly worse outcomes with regard to postoperative ventilation time, re-operation, blood transfusion and length of hospital stay, operative mortality was not statistically different between the two groups (3.4% for RD group vs. 2.3% for the control group), probably because of small sample size. However, Filsoufi et al. reported an increased mortality for patients having SCr of >2.5 mg/dL after single valve replacement (25.0% vs. 2.4%),multiple valve replacement (26.7% vs. 3.4%), and combined valve replacement with CABG (28.0% vs. 4.6%) in a large, single-center cohort (9). Regarding long-term survival, Devbhandari reported 1-, 3- and 5-year survival rates following on-pump coronary bypass surgery as 90.3%, 83.2% and 71.4% for non-dialysis dependent renal dysfunction (NDDRD) patients, and 97.4%, 94.6% and 91.0% for patients with no history of RD, respectively (10). Chronic RD affects not only the operative mortality, but also the morbidity after open heart surgery. It has been shown that preoperative RD is an independent predictor of postoperative acute RD and hemodialysis (HD) (5, 7, 9-12) as well as gastrointestinal (GI) (4, 9), respiratory (5, 9), infectious (5) and neurological (5) complications.

1.2. HEMODIALYSIS:

HD is the most common renal replacement therapy for decades, for those who have end-stage RD and have not received renal transplantation. Intermittent HD is a very efficient method to decrease blood urea and creatinine as well as to treat volume overload. Intermittent HD can be performed temporarily in the setting of acute RD or permanently in the setting of chronic RD. In chronic RD, 3 sessions of 4 hours are usually prescribed to adequately substitute the renal function. A good vascular access is essential to perform HD. A temporary dual- or tri-lumen dialysis catheter has to be inserted into a central vein such as the internal jugular, the subclavian or the femoral vein.

1.3. ULTRAFILTRATION:

Intraoperative ultrafiltration has been used widely in pediatric open heart surgery for decades, reducing total body water, increasing hematocrit (Htc) levels, removing inflammatory mediators, thus improving the operative outcome (13). In the 90's, Naik et al. modified the technique (14), and reported better outcomes with modified ultrafiltration (MUF) in pediatric population (15). However, use of MUF has been limited to end-stage RD patients with volume overload undergoing open heart surgery, as an adjunct to pre- and postoperative HD in the adult population. The Verona group reported fewer respiratory, neurological, GI complications, and less blood product transfusion in the group of patients who received MUF after CPB, however mortality, overall morbidity, length of Intensive Care Unit (ICU) stay and length of hospital stay were comparable between MUF and control groups including 573 consecutive patients (16). A meta-analysis evaluating the effects of ultrafiltration on postoperative blood product use and perioperative bleeding in adult patients revealed fewer bleeding complications and reduced blood product use after intraoperative ultrafiltration (17). Boga et al reported improved cardiac performance after CABG surgery with MUF. However, they could not find any difference in Interleukin-6, Interleukin-8 and Neopterin levels. They attributed this effect to prevention of hemodilution and hypervolemia (18). In summary, no clear evidence is available at the present regarding the impact of intraoperative MUF on the operative outcome of NDDRD patients undergoing open heart surgery. Capuano et al. recently (19) reported successful results in a NDDRD patient who required urgent coronary revascularisation. Nevertheless, the impact of intraoperative MUF on the outcome of NDDRD patients undergoing open heart surgery remains unclear, and is worth investigation.

1.4. PREVIOUS STUDIES:

The quest to improve the outcome of NDDRD patients undergoing open heart surgery has been in the agenda of some groups to date. Two pioneering studies were recently published from Turkey (20, 21). The target patient population was NDDRD patients undergoing elective isolated primary CABG surgery. Patients were randomized into two groups prospectively, one group received 2 doses of prophylactic HD just before surgery whereas the other did not, and served as control. Both studies reported reduced operative mortality rates, reduced postoperative need for HD, and shorter length of stay in the prophylactic HD groups. However, these two studies had very limited number of patients with a short period of follow-up, excluded valve surgery, and did not analyse cost-effectiveness. Furthermore, intraoperative ultrafiltration was not studied.

1.5. ASSESSMENT OF RENAL FUNCTION:

GFR is the best measure of overall kidney function (22). The Cockroft-Gault formula is a commonly used way to predict GFR (23). GFR <30 mL/min/1.73 m2 is accepted as "severe RD" (22). SCr is a simple and practical universal biologic marker used for estimating glomerular filtration. Although SCr does not have a linear association with GFR, it has also been reported to be a powerful predictor of operative mortality (6). Thus, SCr and GFR were both accepted as preoperative indicators of RD with the cut-off levels of 180 µmol/L (or 2.0 mg/dL) and 30 mL/min/1.73 m2, respectively.

1.6. CONCLUSION:

In summary, this data mandates us a well defined strategy for patients with NDDRD in order to obtain better operative outcome. Under the guidance of the current literature, a randomized controlled trial (RCT) with a larger number of patients undergoing open heart surgery will provide precise answers for these questions. Comparison of hospital costs may add an extra value for the assessment of cost-effectiveness as well.

Being tested
Open Heart Surgery (OHS), Intraoperative Modified Ultrafiltration (MUF), Hemodialysis (HD)
Keywords
Renal dysfunction, Hemodialysis, Modified ultrafiltration, Open heart surgery
Medical subject headings
Cardiovascular Diseases, Renal Insufficiency

What participants receive

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

  • Open Heart Surgery (OHS)Procedure or surgery

    General anesthesia, use of iodine impregnated adhesive dressing, median sternotomy and/or thoracotomy incision, full heparinization (300-400 ui/kg), arterial and venous cannulation, initialization of CPB with or without aortic cross-clamping and high-potassium cold cardioplegia, surgical repair under mild-moderate hypothermia. De-clamping (if cross clamp was applied), neutralization of heparin by protamin, de-cannulation and hemostasis after surgical repair. Insertion of drain(s) and pacing wire(s). Closure of all layers in anatomical plan.

  • Intraoperative Modified Ultrafiltration (MUF)Procedure or surgery

    Once the surgical repair is finished, and CPB will be stopped after aortic declamping. The arterial and venous cannulae will be connected to each other using 3-way connectors and a cardioplegia line. When hemodynamic stability is established (MAP >75 mmHg, CVP > 12 mmHg, Htc > 25%), blood will be drained from the arterial cannula using a roller pump, driven to the ultrafilter, and eventually to the venous cannula. The blood flow will be maintained at ~150 mL/min, and suction will be applied to the filtrate port to achieve an ultrafiltration of 100-120 mL/min. Heat exchanger and bubble trap of the cardioplegia line will be used to maintain the filtered blood at body temperature and to prevent air embolism, respectively. MUF will continue 20 minutes. The filtered volume will be collected.

  • Hemodialysis (HD)Procedure or surgery

    Two HD sessions will be performed at 3 days and 1 day prior to surgery. Each session will last 3 hours if the patient weighs < 75 kg, and 4 hours if > 75 kg. Conventional HD will be carried out using a volume-controlled dialysis machine. A bicarbonate dialysate containing K (3 mmol/L), Ca (1.5 mmol/L) and HCO3 (31 mmol/L) will be used. Sodium conductivity will be set at 138 mmol/L. Medium-flow filters will be used as artificial kidney devices. Dialysate temperature will be set at 36oC. Dialysate and blood flow rate will be set at 500 mL/min and 250-300 ml/min, respectively. Intradialytic ultrafiltration will not be used routinely unless the patient has volume overload. The decision to use intradialytic ultrafiltration will be taken with the anaesthesiologist and the cardiac surgeon. If intradialytic ultrafiltration is indicated, maximal rate of ultrafiltration will be 10 ml/kg/hour. These patients will undergo open heart surgery after two sessions of HD.

Study groups in NCT00720967
Study groupRoleWhat they receive
1Active comparatorControl Group (Open heart surgery alone)
Receives: Procedure: Open Heart Surgery (OHS)
2ExperimentalIntraoperative Modified Ultrafiltration (MUF) Group (Open heart surgery with intraoperative MUF)
Receives: Procedure: Open Heart Surgery (OHS); Procedure: Intraoperative Modified Ultrafiltration (MUF)
3ExperimentalPreoperative Hemodialysis Group (Open Heart Surgery after preoperative hemodialysis)
Receives: Procedure: Open Heart Surgery (OHS); Procedure: Hemodialysis (HD)

What is being measured

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

  1. Operative mortality, defined as any death occurring within 30 days after the operation or any death occurring before discharge during the same hospitalization (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

Secondary outcomes (16)
  1. Survival at one year after surgery (in percentage).

    Measured: one year after surgery

  2. Postoperative low cardiac output (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  3. Postoperative permanent neurological deficit (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  4. Postoperative transient neurological deficit (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  5. Postoperative acute renal dysfunction (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  6. Postoperative persistent renal dysfunction requiring hemodialysis (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  7. Postoperative gastrointestinal complication (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  8. Postoperative respiratory failure (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  9. Postoperative systemic infection (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  10. Postoperative local infection (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  11. Postoperative new-onset arrythmia (in percentage).

    Measured: within the first 30 days after surgery or before the discharge after surgery

  12. Postoperative surgical drainage (in mL).

    Measured: within the first 72 hours after surgery

  13. Postoperative need for transfusion of blood products (in unit packs).

    Measured: within the first 72 hours after surgery

  14. Postoperative length of ICU stay (in days)

    Measured: within the first 30 days after surgery or before the discharge after surgery

  15. Postoperative length of hospital stay (in days)

    Measured: within the first 30 days after surgery or before the discharge after surgery

  16. Total hospital costs for the admission of operation (in Euros)

    Measured: From the day of admission to hospital until the day of discharge after surgery

Timeline

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

  1. First posted23 Jul 2008 (estimated)
  2. Study startNov 2008
  3. Primary completionNov 2011 (estimated)
  4. Study completionNov 2012 (estimated)

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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
450 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00720967
Sponsor's protocol ID
08-058 (NAC 08018)
Acronym
SeRenaD-CPB
Status last verified
Jul 2008
First submitted
21 Jul 2008
Last updated
23 Jul 2008
Results posted
No
Data monitoring committee
No

Publications

  • Foley RN, Parfrey PS, Sarnak MJ. Epidemiology of cardiovascular disease in chronic renal disease. J Am Soc Nephrol. 1998 Dec;9(12 Suppl):S16-23.

    PubMed 11443763
  • Schiffrin EL, Lipman ML, Mann JF. Chronic kidney disease: effects on the cardiovascular system. Circulation. 2007 Jul 3;116(1):85-97. doi: 10.1161/CIRCULATIONAHA.106.678342.

    PubMed 17606856
  • Levin A, Foley RN. Cardiovascular disease in chronic renal insufficiency. Am J Kidney Dis. 2000 Dec;36(6 Suppl 3):S24-30. doi: 10.1053/ajkd.2000.19928.

    PubMed 11118155
  • Anderson RJ, O'brien M, MaWhinney S, VillaNueva CB, Moritz TE, Sethi GK, Henderson WG, Hammermeister KE, Grover FL, Shroyer AL. Renal failure predisposes patients to adverse outcome after coronary artery bypass surgery. VA Cooperative Study #5. Kidney Int. 1999 Mar;55(3):1057-62. doi: 10.1046/j.1523-1755.1999.0550031057.x.

    PubMed 10027944
  • Cooper WA, O'Brien SM, Thourani VH, Guyton RA, Bridges CR, Szczech LA, Petersen R, Peterson ED. Impact of renal dysfunction on outcomes of coronary artery bypass surgery: results from the Society of Thoracic Surgeons National Adult Cardiac Database. Circulation. 2006 Feb 28;113(8):1063-70. doi: 10.1161/CIRCULATIONAHA.105.580084. Epub 2006 Feb 20.

    PubMed 16490821
  • Zakeri R, Freemantle N, Barnett V, Lipkin GW, Bonser RS, Graham TR, Rooney SJ, Wilson IC, Cramb R, Keogh BE, Pagano D. Relation between mild renal dysfunction and outcomes after coronary artery bypass grafting. Circulation. 2005 Aug 30;112(9 Suppl):I270-5. doi: 10.1161/CIRCULATIONAHA.104.522623.

    PubMed 16159830
  • Weerasinghe A, Hornick P, Smith P, Taylor K, Ratnatunga C. Coronary artery bypass grafting in non-dialysis-dependent mild-to-moderate renal dysfunction. J Thorac Cardiovasc Surg. 2001 Jun;121(6):1083-9. doi: 10.1067/mtc.2001.113022.

    PubMed 11385375
  • Ibanez J, Riera M, Saez de Ibarra JI, Carrillo A, Fernandez R, Herrero J, Fiol M, Bonnin O. Effect of preoperative mild renal dysfunction on mortality and morbidity following valve cardiac surgery. Interact Cardiovasc Thorac Surg. 2007 Dec;6(6):748-52. doi: 10.1510/icvts.2007.159392. Epub 2007 Sep 21.

    PubMed 17890235
  • Filsoufi F, Rahmanian PB, Castillo JG, Chikwe J, Carpentier A, Adams DH. Early and late outcomes of cardiac surgery in patients with moderate to severe preoperative renal dysfunction without dialysis. Interact Cardiovasc Thorac Surg. 2008 Feb;7(1):90-5. doi: 10.1510/icvts.2007.164483. Epub 2007 Nov 22.

    PubMed 18033787
  • Devbhandari MP, Duncan AJ, Grayson AD, Fabri BM, Keenan DJ, Bridgewater B, Jones MT, Au J; North West Quality Improvement Programme in Cardiac Interventions. Effect of risk-adjusted, non-dialysis-dependent renal dysfunction on mortality and morbidity following coronary artery bypass surgery: a multi-centre study. Eur J Cardiothorac Surg. 2006 Jun;29(6):964-70. doi: 10.1016/j.ejcts.2006.03.038. Epub 2006 May 3.

    PubMed 16675230
  • Kilo J, Margreiter JE, Ruttmann E, Laufer G, Bonatti JO. Slightly elevated serum creatinine predicts renal failure requiring hemofiltration after cardiac surgery. Heart Surg Forum. 2005;8(1):E34-8. doi: 10.1532/HSF98.20041117.

    PubMed 15769711
  • Mangano CM, Diamondstone LS, Ramsay JG, Aggarwal A, Herskowitz A, Mangano DT. Renal dysfunction after myocardial revascularization: risk factors, adverse outcomes, and hospital resource utilization. The Multicenter Study of Perioperative Ischemia Research Group. Ann Intern Med. 1998 Feb 1;128(3):194-203. doi: 10.7326/0003-4819-128-3-199802010-00005.

    PubMed 9454527
  • Shen I, Giacomuzzi C, Ungerleider RM. Current strategies for optimizing the use of cardiopulmonary bypass in neonates and infants. Ann Thorac Surg. 2003 Feb;75(2):S729-34. doi: 10.1016/s0003-4975(02)04697-0.

    PubMed 12607719
  • Naik SK, Knight A, Elliott MJ. A successful modification of ultrafiltration for cardiopulmonary bypass in children. Perfusion. 1991;6(1):41-50. doi: 10.1177/026765919100600106.

    PubMed 10149499
  • Naik SK, Knight A, Elliott M. A prospective randomized study of a modified technique of ultrafiltration during pediatric open-heart surgery. Circulation. 1991 Nov;84(5 Suppl):III422-31.

    PubMed 1934440

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Open Heart Surgery (OHS), Intraoperative Modified Ultrafiltration (MUF) and Hemodialysis (HD) in people with Non-Dialysis Dependent Severe Renal Dysfunction and Cardiovascular Disease, run by University Hospital, Geneva at 7 sites in 5 countries.

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 3 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 23 Jul 2008. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in Turkey (Türkiye), France, Germany, Spain, Switzerland. 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 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

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

Are results available for this study?

Results are not available in the source record.

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

Contact Erman Pektok, MD (+41.76.3169990, epektok@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Operative mortality, defined as any death occurring within 30 days after the operation or any death occurring before discharge during the same hospitalization (in percentage). (time frame: within the first 30 days after surgery or before the discharge after surgery). 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 NCT00720967, which also lists 22 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 Jul 2008; AzTrials last refreshed its copy on 8 Nov 2026.

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