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SMART Study: Sympathetic Mapping/Ablation of Renal Nerves Trial

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Presentation on theme: "SMART Study: Sympathetic Mapping/Ablation of Renal Nerves Trial"— Presentation transcript:

1 SMART Study: Sympathetic Mapping/Ablation of Renal Nerves Trial
----- SyMap Technology Update Jie Wang, MD, PhD Jiangsu Province Hospital Nanjing, China Columbia University, USA

2 Disclosure J Wang is a co-founder of SyMap Medical Ltd
consultant to Coridea, Park Medical

3 Why SYMPLICITY III Missed Its Efficacy Endpoint
Procedure-related factors: Device-related Issue Drug changes/drug adherence Patient population Patients-related Issue 3

4 To Address Device-related Issue:
Our Solution Unique 5-in-1 Catheter/Stimulator/ RF Generator · Systemic Blood Pressure · Heart Rate · Unique 5-in-1 Catheter/ Stimulator/RF Generator 4

5 Novel Catheter and Stimulator/RF Generator

6 To Address Patients-related Issue:
Our Solution Drug Resistant Hypertension Patients? “Real World” Patients (Anti-hypertensive drug therapy for at least 6m, SBP ≧150mmHg, SDP ≧100mmHg)? 6

7 Sympathetic Mapping/Ablation of Renal Nerves Trial
A Prospective, Multicenter, Single Blind, Randomized and Controlled Trial of Renal Sympathetic Denervation Using SyMapCath I™ Catheter and SYMPIONEER S1™ Stimulator/Generator for the Treatment of Hypertension Sympathetic Mapping/Ablation of Renal Nerves Trial (SMART Study) CFDA Registration Trial/13 Hospital/220 Patients Started to Enroll Patients in November, 2016

8 Purpose of the Study To evaluate the safety and efficacy of targeted renal sympathetic denervation in patients with uncontrolled、primary hypertension for at least 6 months, then after standardized drug therapy (at least two drugs) for at least 28 days, office BP is still ≥ 150mmHg, ≤180mmHg

9 Enrollment Criteria: (1)Age≥18 years, ≤65 Year male or female without pregnancy ; (2)Primary hypertension; (3)Office SBP≥ 150mmHg, ≤180mmHg;heart rate at rest ≥ 70bpm without β blocker;Resting HR is not considered if β‐blocker is taken; (4)ASBP measurement ≥135 mmHg; (5)Hypertension history ≥6m; (6)Uncontrolled hypertension with 6m anti-hypertension drug therapy; properly consented; standardized medication (at least two drugs) for at least 28 days before enrollment, office BP≥150mmHg, ≤180mmHg; (7)Consented and willing to accept out-patient follow-up.

10 Study Chart: Consent Uncontrolled Hypertension/at least 6 month Medication, SBP≥150mmHg, ≤180mmHg Lab Tests Running in:standard medication for at least 28 days (at least two drugs) After 28 days of standard medication, Office BP still ≥150mmHg,≤180mmHg,patients are enrolled Lab Tests Renal Angiography 1:1Randomization

11 Assessment of procedure safety Post-Procedure Office BP/24 hour AMBP
1:1Randomlization Renal Ablation N =110 Sham N =110 Assessment of procedure safety Post-Procedure Office BP/24 hour AMBP Within 3 months after the procedure, if SBP mmHg , there are no changes in medication , unless: SBP>160mmHg,increase the drug dose or class according to a strict regimen; SBP<120mmHg,decrease the drug dose or class according to a strict regimen; Or SBP<130mmHg,decrease the drug dose or class according to a strict regimen due to patients showed difficulties to tolerate the drugs.

12 Three months after the procedure:
SBP<120mmmHg,reduce anti-hypertension drugs; SBP<140mmmHg,no changes in drug regimen; Uncontrolled SBP,medication changes according to a strict drug regimen Follow-up: Office BP and urine sample 7days, 1m, 2m, 3m, 4m, 5m, 6m, 9m and 12m after the procedure. CTA and 24-hour ambulatory BP The changes in medications are determined by follow-up physicians ; Follow-up physicians and procedure performance physicians are blind each other; Drug adherence is monitored by HPLC- MS/MS (urine samples); The study will be performed at 16 hospitals.

13 Primary Efficacy Endpoints
The Control Rate of Office SBP ( SBP<140mmHg) at 6 month after the treatment The composite index of anti-hypertension drugs at 6 months after the treatments Composite Index based on the class numbers and doses of medications: Composite Index = Weights X ( sum of doses) # Classes: Weights; Dose: Factors One Standard Dose is defined as 1; Half dose: 0.5,Double Dose: 2 , et al Examples: Two classes of drugs were taken,double doses were used for one class and half dose was used for another class: The Index = 2*(2+0.5)=5 ; Five classes of drugs were taken ,one standard dose was used for each class, respectively, The Index = 5*( )=25 Weights 1 Class 1 2 Classes 2 3 Classes 3 4 Classes 4 5 Classes 5

14 Secondary Efficacy Endpoints:
The Change in mean 24-hour Ambulatory Systolic Blood Pressure Measurement at month 6 The change in mean 24 hour Ambulatory Systolic, Diastolic and Mean Arterial Pressure at 24 hours after the treatment Office BP at 1m、2m、3m、4m、5m、6m、9m、12 m after the treatment; The composite index of anti-hypertension drugs at 1m、2 m 、3m、4m、5m、9m、12m after the treatment

15 Safety Endpoints MASE Cardiac function Renal function

16 Standardization of Anti-hypertension Drug Regimen
Standardized Drugs, Doses and Manufacture: Class Name Commercial Name Manufacture Standard Dose Maximum Dose 1 ARB Irbesartan Aprovel/ 安博维 Sannofi(Hanzhou, China) 150mg/Day 300mg/Day 2 CCB Amlodipine Norvasc/ 络活喜 Pfizer(Dalian, China) 5mg/Day 10mg/Day 3 Β Receptor Blocker Metoprolol Sustained Release Betaloc Zok/倍他乐克 缓释片 AstraZeneca 47.5mg/Day 95mg/Day 4 Diuretic Hydrochlorothiazide 氢氯噻嗪片 Changzhou Pharmaceutical 25mg/Day 50mg/Day 5 α Receptor Blocker Terazosin Hydrochloride 高特灵 Abbott (Shanghai) 2mg/Day 4mg/Day 6 Combination Drug Irbesartan+ Coaprovel/ 安博诺 Sanofi(Hanzhou, China) Irbesartan 150mg+ Hydrochlo. 12.5mg/Day Irbesartan 300mg+Hydrochlo 25mg/Day

17 Running In Period The first visit: SBP≥150mmHg,≤180mmHg: A.Patient with one drug:need add another class drug,ARB is the first choice. If CCB is taken, ARB will be added; if ARB is taken, CCB will be added; if other class of drug is taken this drug must be replaced by the same class of drug and add ARB. B.Patient with two drugs: these two drugs need to be replaced by drugs/doses in the Regimen. In the case patient still has severe complains and diuretic is not taken, diuretic or Coaprovel is added. C.Patients with three drugs: these three drugs are switched to the same classes of drugs in the list of Standardization of Drug Regimen with defined doses. D.Patient with combined drug: it should switch to Coaprovel; If BP is still uncontrolled and patient has severe complains, CCB will be added. E. If ACEI is used , it needs to replaced by ARB. F. The standardized anti-hypertension drug therapy much be performed for at least 28 days.

18 A Strict Regimen for Post-randomization
Medication Changes Regimen to Add Drugs:Increase in dosing is firstly selected until defined maximum dose; if systolic BP is still not controlled, then another class drug is added according to the order as above . If the class of drug is not proper to the patient evidenced by clinical signs the class can be escaped and next class of drug is used. For instance, patient with irbesartan 50mg/day + Amlodipine 5mg/day,SBP is still >160mmHg. HR is < 65 b/min,Metoprolol will be escaped and hydrochlorothiazide is used。 Regimen to Reduce Drugs: Decrease in dosing is considered firstly; if it is needed then the class of drug is reduced according to above order。 Order to Add Drugs Irbesartan Amlodipine Metoprolol Hydro-chlorothiazide Terzzosin Hydrochloride Order to Reduce Drugs

19 Renal Sympathetic Mapping/Ablation
Right Left Before Mapping/Ablation During Mapping/Ablation After Mapping/Ablation

20 Preliminary Data N=4 Left Renal A. Right Renal A. Total Mapping 23 26
Left Renal A. Right Renal A. Total Mapping 23 26 49 Average 5.75 6.5 Hot Sites  13  16 29  3.25 4 % 57 62 59 2nd Ablation 5 7 12 39 43 41

21 Changes in BP in Responses to Renal Stimulations
The Responses of Blood Pressure to Renal Stimulation Before Renal Ablation SBP (mmHg) Before After △SBP DBP △DBP MAP △MAP Mean 160 179 19 86 95 9 111 122 11 SE 4.0 4.9 2.2 3.7 3.8 1.1 2.4 2.6 1.2 The Responses of Blood Pressure to Renal Stimulation After Renal Ablation Effective Ablation:26/29=90% △DBP (mmHg) △MAP(mmHg) 162 167 5 89 90 3 110 116 4.6 4.7 1.9 3.9 4.1 1.0 0.9

22 Preliminary Data 28 Days of Standard Drug Therapy
Time Office BP mmHg Heart Rate b/min 09:09:53 156/108 102 09:11:53 155/101 104 09:13:21 165/105 103 Mean 162/103 24 Hour AMBP: Systolic: Max184mmHg Min137 mmHg Mean 161mmHg Diastolic:Max 123mmHg Min 049mmHg Mean 097mmHg 5 Days after the Procedure Time Office BP mmHg Heart Rate b/min 13:52:33 145/097 91 13:53:38 145/096 92 13:54:51 140/079 90 Mean 143/091 24 Hour AMBP: Systolic: Max 216mmHg  Min112 mmHg  Mean 147mmHg Diastolic:Max 158mmHg  Min 57mmHg  Mean 99mmHg

23 Preliminary Data One Month after the Procedure
Time Office BP mmHg Heart Rate b/min 09:01:19 144/102 NA 09:02:35 142/97 09:03:42 138/90 Mean 141/96 105 Two Months after the Procedure Time Office BP mmHg Heart Rate b/min 09:08:29 125/88 NA 09:09:35 134/88 09:10:43 140/89 Mean 133/88 104

24 Summary Targeted Renal Sympathetic Denervation
Proper Patient Population Not intend to “bit” drug therapy; as an alternative therapy to address issues of drug therapy Waiting for more results

25 Thank You


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