Heart DiseasesNCT00005199
Balloon Valvuloplasty Registry
An observational study of Heart Diseases and Mitral Valve Stenosis, run by National Heart, Lung, and Blood Institute (NHLBI).
Trial summary
To establish a registry in order to collect and analyze baseline and outcome data on patients with severe valvular stenosis treated with balloon valvuloplasty. Read more about this study
- Who is it for?
- Any age, men only
- Conditions the study is for
- Heart Diseases, Mitral Valve Stenosis, Aortic Valve Stenosis
- How many people
- Not given
- Where
- No sites listed yet
- Study dates
- Jun 1987to Nov 1994
- Phase
- Observational
- 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 Any age
- Men only
- No healthy volunteers
- Child, Adult, Older adult
No eligibility criteria
About this study
To establish a registry in order to collect and analyze baseline and outcome data on patients with severe valvular stenosis treated with balloon valvuloplasty.
Read the detailed description
BACKGROUND:
Valvular stenosis or incompetence results in an estimated 41,000 valve replacements in the United States each year. These replacements are equally distributed between the aortic and mitral valves. An estimated 60 percent of aortic valve replacements are the result of valve stenosis; 20-30 percent of mitral valve replacements are due to stenosis. The risk of operative mortality in single valve replacement ranges from 3 percent to as high as 15 percent depending upon patient characteristics. Morbidity associated with open heart procedures includes wound infection, reoperation for bleeding, and post-operative pain. Most patients with artificial valves require anticoagulant therapy for the rest of their lives and thus face the competing risks of hemorrhage and valve thrombosis/embolism. In addition, there are a number of patients with aortic stenosis who are not candidates for aortic valve replacement because of unacceptable operative risks who might be dramatically improved by balloon valvuloplasty.
The pathophysiologic processes underlying valvular stenosis at the aortic and mitral positions are quite different. Mitral stenosis is an outcome of rheumatic fever. Rheumatic fever is quite unusual in this country but it and its sequelae, rheumatic valvular disease, persist as major public health problems in the Third World. Aortic stenosis is most commonly the result of calcific degeneration of a normal tricuspid aortic valve in the elderly or the result of rheumatic fever but can also develop in a congenital bicuspid aortic valve which becomes progressively more stenotic with age and the wear of abnormal flow patterns.
The results of surgical valvuloplasty differ for mitral and aortic valves. Surgical valvuloplasty (commissurotomy) for mitral stenosis is currently a well-established and commonly used treatment for symptomatic patients with mitral stenosis. Similar attempts at repair of aortic stenosis have been largely unsuccessful. Surgical valvuloplasty for aortic stenosis has, for this reason, been abandoned in favor of valve replacement. Initial attempts at aortic balloon valvuloplasty were, therefore, undertaken in patients who were not surgical candidates; these initial efforts in a small number of patients, coming as they did in the wake of abandoned surgical attempts, were surprisingly successful in reducing gradients and increasing valve area without complications such as embolism or significant regurgitation.
Balloon valvuloplasty began with pediatric cardiologists using catheters designed for dilatation of peripheral arterial stenosis in children with pulmonic stenosis and those with coarctation of the aorta. Balloon dilatation has been quite successful with pulmonic stenosis, and is now an accepted therapeutic maneuver. It is less successful with coarctation of the aorta. As a direct outgrowth of this research, investigators have applied this procedure to mitral and aortic stenosis in adults.
Balloon valvuloplasty is performed in the cardiac catheterization laboratory without general anesthesia. A balloon catheter is inserted percutaneously in the venous side of the circulation and is placed across the mitral valve after puncture of the atrial septum. Inflation of appropriately sized balloons has resulted in marked reduction of transvalvular gradients and increase in calculated valve area in most of the cases thus far reported. Given the success of closed commissurotomy, these are not surprising findings.
A similar procedure has been used in severely stenotic aortic valves by either advancing the balloon through the mitral valve into the aortic position or approaching the valve retrograde. Aortic balloon valvuloplasty has thus far been employed largely in severely ill, elderly patients who are judged not able to tolerate valve replacement. As noted above, results have been quite promising; low mortality and morbidity, substantial hemodynamic improvement and short hospital stays have been observed. These anecdotal reports have led to the application of balloon valvuloplasty in increasing numbers of patients. Major issues needed to be addressed prior to general acceptance of this therapy for both aortic and mitral stenosis and for operative and nonoperative candidates. The issues include: definition of risk of mortality and morbidity overall and in subgroups defined by baseline characteristics; success rate defined clinically and hemodynamically overall and in subgroups; the durability of this procedure, that is, how long will a given improvement in clinical and hemodynamic measures persist; definition of subgroups with particularly favorable or unfavorable outcomes. These questions were addressed by the NHLBI Balloon Valvuloplasty Registry.
DESIGN NARRATIVE:
Investigators treating patients with balloon valvuloplasty voluntarily collected and submitted data on consecutive cases of valvuloplasty for two years of active recruitment and followed patients at selected intervals for a minimum of two and a half years. Demographic, clinical, and hemodynamic data were collected on each patient during the valvuloplasty hospitalization. The data were submitted from the participating clinical units to the Coordinating Center.
- Conditions
- Heart Diseases, Mitral Valve Stenosis, Aortic Valve Stenosis
- Medical subject headings
- Heart Diseases, Mitral Valve Stenosis, Aortic Valve Stenosis
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2000 (estimated)
- Study startJun 1987
- Study completionNov 1994
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (11)Papers the sponsor has linked to this study.
- Other trials for Heart DiseasesStudies of the same condition, open and under way.
- More trials run by National Heart, Lung, and Blood Institute (NHLBI)The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
Sponsor and investigators
- Sponsor type
- US National Institutes of Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00005199
- Sponsor's protocol ID
- 1078
- Status last verified
- May 2000
- First submitted
- 25 May 2000
- Last updated
- 24 Jun 2005
- Results posted
- No
Publications
Reid CL, Otto CM, Davis KB, Labovitz A, Kisslo KB, McKay CR. Influence of mitral valve morphology on mitral balloon commissurotomy: immediate and six-month results from the NHLBI Balloon Valvuloplasty Registry. Am Heart J. 1992 Sep;124(3):657-65. doi: 10.1016/0002-8703(92)90274-y.
PubMed 1514494Davidson CJ, Bashore TM, Mickel M, Davis K. Balloon mitral commissurotomy after previous surgical commissurotomy. The National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry participants. Circulation. 1992 Jul;86(1):91-9. doi: 10.1161/01.cir.86.1.91.
PubMed 1617794Otto CM, Davis KB, Holmes DR Jr, O'Neill W, Ferguson J, Bashore TM, Bonan R. Methodologic issues in clinical evaluation of stenosis severity in adults undergoing aortic or mitral balloon valvuloplasty. The NHLBI Balloon Valvuloplasty Registry. Am J Cardiol. 1992 Jun 15;69(19):1607-16. doi: 10.1016/0002-9149(92)90712-8.
PubMed 1598878Complications and mortality of percutaneous balloon mitral commissurotomy. A report from the National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry. Circulation. 1992 Jun;85(6):2014-24. doi: 10.1161/01.cir.85.6.2014.
PubMed 1591821Multicenter experience with balloon mitral commissurotomy. NHLBI Balloon Valvuloplasty Registry Report on immediate and 30-day follow-up results. The National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry Participants. Circulation. 1992 Feb;85(2):448-61. doi: 10.1161/01.cir.85.2.448.
PubMed 1735143Otto CM, Nishimura RA, Davis KB, Kisslo KB, Bashore TM. Doppler echocardiographic findings in adults with severe symptomatic valvular aortic stenosis. Balloon Valvuloplasty Registry Echocardiographers. Am J Cardiol. 1991 Dec 1;68(15):1477-84. doi: 10.1016/0002-9149(91)90282-p.
PubMed 1746430Percutaneous balloon aortic valvuloplasty. Acute and 30-day follow-up results in 674 patients from the NHLBI Balloon Valvuloplasty Registry. Circulation. 1991 Dec;84(6):2383-97. doi: 10.1161/01.cir.84.6.2383.
PubMed 1959194Otto CM, Mickel MC, Kennedy JW, Alderman EL, Bashore TM, Block PC, Brinker JA, Diver D, Ferguson J, Holmes DR Jr, et al. Three-year outcome after balloon aortic valvuloplasty. Insights into prognosis of valvular aortic stenosis. Circulation. 1994 Feb;89(2):642-50. doi: 10.1161/01.cir.89.2.642.
PubMed 8313553Otto CM, Davis KB, Reid CL, Slater JN, Kronzon I, Kisslo KB, Bashore TM. Relation between pulmonary artery pressure and mitral stenosis severity in patients undergoing balloon mitral commissurotomy. Am J Cardiol. 1993 Apr 1;71(10):874-8. doi: 10.1016/0002-9149(93)90844-3. No abstract available.
PubMed 8456774Douglas PS, Otto CM, Mickel MC, Labovitz A, Reid CL, Davis KB. Gender differences in left ventricle geometry and function in patients undergoing balloon dilatation of the aortic valve for isolated aortic stenosis. NHLBI Balloon Valvuloplasty Registry. Br Heart J. 1995 Jun;73(6):548-54. doi: 10.1136/hrt.73.6.548.
PubMed 7626355Engbaek F, Voldby B. Radioimmunoassay of serotonin (5-hydroxytryptamine) in cerebrospinal fluid, plasma, and serum. Clin Chem. 1982 Apr;28(4 Pt 1):624-8.
PubMed 7074830
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2005. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Balloon Valvuloplasty Registry
- ClinicalTrials.gov ID
- NCT00005199
- Acronym / sponsor ID
- 1078
- Conditions
- Heart Diseases, Mitral Valve Stenosis, Aortic Valve Stenosis
- Study type
- Observational
- Recruitment status
- Completed
- Lead sponsor
- National Heart, Lung, and Blood Institute (NHLBI)US National Institutes of Health
- Study start
- Jun 1987
- Study completion
- Nov 1994
- First posted
- 26 May 2000 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To establish a registry in order to collect and analyze baseline and outcome data on patients with severe valvular stenosis treated with balloon valvuloplasty.
Detailed description
BACKGROUND:
Valvular stenosis or incompetence results in an estimated 41,000 valve replacements in the United States each year. These replacements are equally distributed between the aortic and mitral valves. An estimated 60 percent of aortic valve replacements are the result of valve stenosis; 20-30 percent of mitral valve replacements are due to stenosis. The risk of operative mortality in single valve replacement ranges from 3 percent to as high as 15 percent depending upon patient characteristics. Morbidity associated with open heart procedures includes wound infection, reoperation for bleeding, and post-operative pain. Most patients with artificial valves require anticoagulant therapy for the rest of their lives and thus face the competing risks of hemorrhage and valve thrombosis/embolism. In addition, there are a number of patients with aortic stenosis who are not candidates for aortic valve replacement because of unacceptable operative risks who might be dramatically improved by balloon valvuloplasty.
The pathophysiologic processes underlying valvular stenosis at the aortic and mitral positions are quite different. Mitral stenosis is an outcome of rheumatic fever. Rheumatic fever is quite unusual in this country but it and its sequelae, rheumatic valvular disease, persist as major public health problems in the Third World. Aortic stenosis is most commonly the result of calcific degeneration of a normal tricuspid aortic valve in the elderly or the result of rheumatic fever but can also develop in a congenital bicuspid aortic valve which becomes progressively more stenotic with age and the wear of abnormal flow patterns.
The results of surgical valvuloplasty differ for mitral and aortic valves. Surgical valvuloplasty (commissurotomy) for mitral stenosis is currently a well-established and commonly used treatment for symptomatic patients with mitral stenosis. Similar attempts at repair of aortic stenosis have been largely unsuccessful. Surgical valvuloplasty for aortic stenosis has, for this reason, been abandoned in favor of valve replacement. Initial attempts at aortic balloon valvuloplasty were, therefore, undertaken in patients who were not surgical candidates; these initial efforts in a small number of patients, coming as they did in the wake of abandoned surgical attempts, were surprisingly successful in reducing gradients and increasing valve area without complications such as embolism or significant regurgitation.
Balloon valvuloplasty began with pediatric cardiologists using catheters designed for dilatation of peripheral arterial stenosis in children with pulmonic stenosis and those with coarctation of the aorta. Balloon dilatation has been quite successful with pulmonic stenosis, and is now an accepted therapeutic maneuver. It is less successful with coarctation of the aorta. As a direct outgrowth of this research, investigators have applied this procedure to mitral and aortic stenosis in adults.
Balloon valvuloplasty is performed in the cardiac catheterization laboratory without general anesthesia. A balloon catheter is inserted percutaneously in the venous side of the circulation and is placed across the mitral valve after puncture of the atrial septum. Inflation of appropriately sized balloons has resulted in marked reduction of transvalvular gradients and increase in calculated valve area in most of the cases thus far reported. Given the success of closed commissurotomy, these are not surprising findings.
A similar procedure has been used in severely stenotic aortic valves by either advancing the balloon through the mitral valve into the aortic position or approaching the valve retrograde. Aortic balloon valvuloplasty has thus far been employed largely in severely ill, elderly patients who are judged not able to tolerate valve replacement. As noted above, results have been quite promising; low mortality and morbidity, substantial hemodynamic improvement and short hospital stays have been observed. These anecdotal reports have led to the application of balloon valvuloplasty in increasing numbers of patients. Major issues needed to be addressed prior to general acceptance of this therapy for both aortic and mitral stenosis and for operative and nonoperative candidates. The issues include: definition of risk of mortality and morbidity overall and in subgroups defined by baseline characteristics; success rate defined clinically and hemodynamically overall and in subgroups; the durability of this procedure, that is, how long will a given improvement in clinical and hemodynamic measures persist; definition of subgroups with particularly favorable or unfavorable outcomes. These questions were addressed by the NHLBI Balloon Valvuloplasty Registry.
DESIGN NARRATIVE:
Investigators treating patients with balloon valvuloplasty voluntarily collected and submitted data on consecutive cases of valvuloplasty for two years of active recruitment and followed patients at selected intervals for a minimum of two and a half years. Demographic, clinical, and hemodynamic data were collected on each patient during the valvuloplasty hospitalization. The data were submitted from the participating clinical units to the Coordinating Center.
Study design
Who may qualify
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2005.
- Background: PubMed 1514494Reid CL, Otto CM, Davis KB, Labovitz A, Kisslo KB, McKay CR. Influence of mitral valve morphology on mitral balloon commissurotomy: immediate and six-month results from the NHLBI Balloon Valvuloplasty Registry. Am Heart J. 1992 Sep;124(3):657-65. doi: 10.1016/0002-8703(92)90274-y.
- Background: PubMed 1617794Davidson CJ, Bashore TM, Mickel M, Davis K. Balloon mitral commissurotomy after previous surgical commissurotomy. The National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry participants. Circulation. 1992 Jul;86(1):91-9. doi: 10.1161/01.cir.86.1.91.
- Background: PubMed 1598878Otto CM, Davis KB, Holmes DR Jr, O'Neill W, Ferguson J, Bashore TM, Bonan R. Methodologic issues in clinical evaluation of stenosis severity in adults undergoing aortic or mitral balloon valvuloplasty. The NHLBI Balloon Valvuloplasty Registry. Am J Cardiol. 1992 Jun 15;69(19):1607-16. doi: 10.1016/0002-9149(92)90712-8.
- Background: PubMed 1591821Complications and mortality of percutaneous balloon mitral commissurotomy. A report from the National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry. Circulation. 1992 Jun;85(6):2014-24. doi: 10.1161/01.cir.85.6.2014.
- Background: PubMed 1735143Multicenter experience with balloon mitral commissurotomy. NHLBI Balloon Valvuloplasty Registry Report on immediate and 30-day follow-up results. The National Heart, Lung, and Blood Institute Balloon Valvuloplasty Registry Participants. Circulation. 1992 Feb;85(2):448-61. doi: 10.1161/01.cir.85.2.448.
- Background: PubMed 1746430Otto CM, Nishimura RA, Davis KB, Kisslo KB, Bashore TM. Doppler echocardiographic findings in adults with severe symptomatic valvular aortic stenosis. Balloon Valvuloplasty Registry Echocardiographers. Am J Cardiol. 1991 Dec 1;68(15):1477-84. doi: 10.1016/0002-9149(91)90282-p.
- Background: PubMed 1959194Percutaneous balloon aortic valvuloplasty. Acute and 30-day follow-up results in 674 patients from the NHLBI Balloon Valvuloplasty Registry. Circulation. 1991 Dec;84(6):2383-97. doi: 10.1161/01.cir.84.6.2383.
- Background: PubMed 8313553Otto CM, Mickel MC, Kennedy JW, Alderman EL, Bashore TM, Block PC, Brinker JA, Diver D, Ferguson J, Holmes DR Jr, et al. Three-year outcome after balloon aortic valvuloplasty. Insights into prognosis of valvular aortic stenosis. Circulation. 1994 Feb;89(2):642-50. doi: 10.1161/01.cir.89.2.642.
- Background: PubMed 8456774Otto CM, Davis KB, Reid CL, Slater JN, Kronzon I, Kisslo KB, Bashore TM. Relation between pulmonary artery pressure and mitral stenosis severity in patients undergoing balloon mitral commissurotomy. Am J Cardiol. 1993 Apr 1;71(10):874-8. doi: 10.1016/0002-9149(93)90844-3. No abstract available.
- Background: PubMed 7626355Douglas PS, Otto CM, Mickel MC, Labovitz A, Reid CL, Davis KB. Gender differences in left ventricle geometry and function in patients undergoing balloon dilatation of the aortic valve for isolated aortic stenosis. NHLBI Balloon Valvuloplasty Registry. Br Heart J. 1995 Jun;73(6):548-54. doi: 10.1136/hrt.73.6.548.
- Background: PubMed 7074830Engbaek F, Voldby B. Radioimmunoassay of serotonin (5-hydroxytryptamine) in cerebrospinal fluid, plasma, and serum. Clin Chem. 1982 Apr;28(4 Pt 1):624-8.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Heart Diseases and Mitral Valve Stenosis, run by National Heart, Lung, and Blood Institute (NHLBI).
The full registered description is in the About this study section and the official record.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jun 2005. Status can change between updates, so confirm with the study contact before making plans.
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.
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.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00005199, which also lists 11 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 24 Jun 2005.