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The Effect of Nitrendipine/Atenolol Combination on Blood Pressure Variability.

Primary Purpose

Hypertension

Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Nitrendipine/Atenolol
Nitrendipine
Atenolol
Sponsored by
Shanghai Jiao Tong University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension focused on measuring blood pressure variability, nitrendipine, atenolol

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men or Women.
  • Aged 30-65 years.
  • Ambulatory systolic blood pressure ≥ 135 mmHg and/or diastolic blood pressure ≥ 85 mmHg.
  • Ambulatory daytime systolic blood pressure standard deviation (SD)≥13mmHg.
  • Never took antihypertensive drugs.
  • Signed the written consent.

Exclusion Criteria:

  • Under antihypertensive treatments.
  • Clinic systolic blood pressure ≥ 160mmHg and/or diastolic blood pressure ≥ 100mmHg.
  • Contraindications to the treatment of drugs, including hypersensitivity reaction, bradycardia, asthma, etc.
  • Any cardiovascular disease except hypertension.
  • Suspected or confirmed secondary hypertension.
  • Poor compliance.

Sites / Locations

  • Shanghai Institite of Hypertension, Ruijin Hospital, Shanghai Jiao Tong University School of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Sequence 1

Sequence 2

Arm Description

One pill of nitrendipine/atenolol combination (5/10mg) once daily for 6 weeks first, and followed by monotherapy for another 6 weeks, when patients will evenly assigned to one pill of nitrendipine (10mg) or one pill of atenolol (25mg) once daily.

Monotherapy for 6 weeks first, when patients will evenly assigned to one pill of nitrendipine (10mg) or one pill of atenolol (25mg) once daily, followed by one pill of nitrendipine/atenolol combination (5/10mg) once daily for another 6 weeks.

Outcomes

Primary Outcome Measures

Ambulatory systolic blood pressure variability 1
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Ambulatory systolic blood pressure variability 2
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).

Secondary Outcome Measures

Ambulatory diastolic blood pressure variability 1
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Ambulatory diastolic blood pressure variability 2
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Ambulatory blood pressure 1
Including ambulatory blood pressure over 24 hours, daytime and nighttime.
Ambulatory blood pressure 2
Including ambulatory blood pressure over 24 hours, daytime and nighttime.

Full Information

First Posted
May 27, 2021
Last Updated
April 11, 2023
Sponsor
Shanghai Jiao Tong University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04931108
Brief Title
The Effect of Nitrendipine/Atenolol Combination on Blood Pressure Variability.
Official Title
The Effect of Nitrendipine/Atenolol Combination on Blood Pressure Variability of Patients With Grade 1 Hypertension Compared With Nitrendipine or Atenolol Monotherapy.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 27, 2021 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Jiao Tong University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Study name: The Effect of Nitrendipine/Atenolol Combination on Blood Pressure Variability. Medicine: Nitrendipine/Atenolol; Nitrendipine; Atenolol. Rationale: Blood pressure variability correlates with cardiovascular events and target-organ damage in hypertensive patients. Nitrendipine/Atenolol has obvious advantages in reducing blood pressure variability in hypertensive rats, but the effect of this combination on hypertensive patients is still unknown. Objective: To evaluate the effect of nitrendipine/atenolol on blood pressure variability of patients with Grade 1 hypertension compared with nitrendipine or atenolol monotherapy. Study design: This study is a cross-over, randomized, controlled clinical trial with two equally sized treatment groups: Nitrendipine/Atenolol (5mg/10mg); Nitrendipine (10mg) or atenolol (25mg). Study population: Men and Women aged 30-65 years (n=32) meeting the inclusion/exclusion criteria. Randomization and cross-over design: Eligible patients will be randomly divided into two groups. Half of patients will take nitrendipine/atenolol (5/10mg) once daily for 6 weeks first, and then evenly turn into nitrendipine (10mg) or atenolol (25mg) once daily for 6 weeks. Another half of patients will evenly take nitrendipine (10mg) or atenolol (25mg) first, and turn into nitrendipine/atenolol (5/10mg) next. Follow up: 14 weeks. Sample size: a total of 32 patients should be enrolled. Timeline: After obtaining the approval of Ethics Committee of Ruijin Hospital in April 2021, recruitment will start. Patients enrollment and follow-up will be performed between June 2021 to June 2022.
Detailed Description
Study name: The effect of Nitrendipine/Atenolol combination on blood pressure variability of patients with Grade 1 hypertension compared with nitrendipine or atenolol monotherapy. Medicine: Nitrendipine/Atenolol (5/10mg tablet); Nitrendipine (10mg tablet); Atenolol (25mg tablet) Rationale: Blood pressure variability correlates with cardiovascular events and target-organ damage in hypertensive patients. Nitrendipine/Atenolol has obvious advantages in reducing blood pressure variability in hypertensive rats, but the effect of this combination on hypertensive patients is still unknown. Objective: To evaluate the effect of nitrendipine/atenolol on blood pressure variability of patients with Grade 1 hypertension compared with nitrendipine or atenolol monotherapy. Study design: This study is a cross-over, randomized, controlled clinical trial with two equally sized treatment groups: Nitrendipine/Atenolol (5mg/10mg); Nitrendipine (10mg) or atenolol (25mg). Study population: Eligible patients (n=32) should be men or women aged 30-65 years. Untreated patients diagnosed as essential hypertension, whose daytime systolic blood pressure ≥ 135mmHg and/or daytime diastolic blood pressure ≥ 85mmHg, and standard deviation (SD)≥13mmHg will be recruited. Randomization and cross-over design: Eligible patients will be randomly divided into two groups. Half of patients will take nitrendipine/atenolol (5/10mg) once daily for 6 weeks first, and then evenly turn into nitrendipine (10mg) or atenolol (25mg) once daily for 6 weeks. Another half of patients will evenly take nitrendipine (10mg) or atenolol (25mg) first, and turn into nitrendipine/atenolol (5/10mg) next. Follow up: 14 weeks. 1 week for screening period, 6 weeks for the first period of treatment, 1 week for wash-out period, and 6 weeks for the second period of treatment. Sample size: a total of 32 patients should be enrolled. Timeline: After obtaining the approval of Ethics Committee of Ruijin Hospital in April 2021, recruitment will start. Patients enrollment and follow-up will be performed between June 2021 to June 2022. Organization: The Centre for Epidemiological Studies and Clinical Trials, Ruijin Hospital, Shanghai, China.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension
Keywords
blood pressure variability, nitrendipine, atenolol

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Half of patients will take nitrendipine/atenolol (5/10mg) once daily for 6 weeks first, and then evenly turn into nitrendipine (10mg) or atenolol (25mg) once daily for 6 weeks. Another half of patients will evenly take nitrendipine (10mg) or atenolol (25mg) first, and turn into nitrendipine/atenolol (5/10mg) next.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sequence 1
Arm Type
Experimental
Arm Description
One pill of nitrendipine/atenolol combination (5/10mg) once daily for 6 weeks first, and followed by monotherapy for another 6 weeks, when patients will evenly assigned to one pill of nitrendipine (10mg) or one pill of atenolol (25mg) once daily.
Arm Title
Sequence 2
Arm Type
Experimental
Arm Description
Monotherapy for 6 weeks first, when patients will evenly assigned to one pill of nitrendipine (10mg) or one pill of atenolol (25mg) once daily, followed by one pill of nitrendipine/atenolol combination (5/10mg) once daily for another 6 weeks.
Intervention Type
Drug
Intervention Name(s)
Nitrendipine/Atenolol
Other Intervention Name(s)
Nitrendipine and Atenolol Tablets
Intervention Description
Nitrendipine/Atenolol 5mg/10mg single-pill combination, oral tablet, one pill daily.
Intervention Type
Drug
Intervention Name(s)
Nitrendipine
Other Intervention Name(s)
Nitrendipine Tablets
Intervention Description
Nitrendipine 5mg, oral tablet, one pill daily.
Intervention Type
Drug
Intervention Name(s)
Atenolol
Other Intervention Name(s)
Atenolol Tablets
Intervention Description
Atenolol 25mg, oral tablet, one pill daily.
Primary Outcome Measure Information:
Title
Ambulatory systolic blood pressure variability 1
Description
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Time Frame
The first 6 weeks of treatment.
Title
Ambulatory systolic blood pressure variability 2
Description
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Time Frame
The second 6 weeks of cross-over treatment.
Secondary Outcome Measure Information:
Title
Ambulatory diastolic blood pressure variability 1
Description
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Time Frame
The first 6 weeks of treatment.
Title
Ambulatory diastolic blood pressure variability 2
Description
Including the average real variability (ARV), the coefficient of variation (CV),and the standard deviation (SD).
Time Frame
The second 6 weeks of cross-over treatment.
Title
Ambulatory blood pressure 1
Description
Including ambulatory blood pressure over 24 hours, daytime and nighttime.
Time Frame
The first 6 weeks of treatment.
Title
Ambulatory blood pressure 2
Description
Including ambulatory blood pressure over 24 hours, daytime and nighttime.
Time Frame
The second 6 weeks of cross-over treatment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men or Women. Aged 30-65 years. Ambulatory systolic blood pressure ≥ 135 mmHg and/or diastolic blood pressure ≥ 85 mmHg. Ambulatory daytime systolic blood pressure standard deviation (SD)≥13mmHg. Never took antihypertensive drugs. Signed the written consent. Exclusion Criteria: Under antihypertensive treatments. Clinic systolic blood pressure ≥ 160mmHg and/or diastolic blood pressure ≥ 100mmHg. Contraindications to the treatment of drugs, including hypersensitivity reaction, bradycardia, asthma, etc. Any cardiovascular disease except hypertension. Suspected or confirmed secondary hypertension. Poor compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiguang Wang, MD, PhD
Phone
+86-21-64370045
Ext
610911
Email
jiguangw@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiguang Wang, MD, PhD
Organizational Affiliation
Shanghai Institite of Hypertension, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shanghai Institite of Hypertension, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiguang Wang, MD, PhD
Phone
86-21-64370045
Ext
610911
Email
jiguangw@163.com

12. IPD Sharing Statement

Learn more about this trial

The Effect of Nitrendipine/Atenolol Combination on Blood Pressure Variability.

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