Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:38 AM
Ignite Modification Date:
2025-12-25 @ 3:38 AM
NCT ID:
NCT02235402
Eligibility Criteria:
Inclusion Criteria:
* Age 18 or over
* Hypertensive at screening: Diastolic blood pressure (DBP) 95 - 115 mm Hg and / or systolic blood pressure (SBP) \>= 160 mm Hg on no therapy or on monotherapy. If currently on monotherapy, DBP could have been \< 95 mm Hg and SBP \< 160 mm Hg, but the patient must have been experiencing unacceptable side effects from their current treatment. Patient must then be able to stop treatment for the placebo run in phase of four weeks without endangering their health (at investigator's discretion)
* Hypertensive at randomisation: DBP 95-115 mm Hg and or SBP \>=160
* Able to give written informed consent
Exclusion Criteria:
* Grad III or grad IV hypertensive retinopathy
* Renal impairment; serum creatinine \> 150 µmol/L
* Heart failure. (New York Heart Association (NYHA) Class III or IV)
* Liver impairment (abnormal Liver function test (LFT) with aspartate-amino transferase (AST) / alanine-amino transferase (ALT) \> 2x upper normal limit or bilirubin \> 2x upper normal limit)
* Recent (\< 2 months) history of unstable angina
* Recent (\< 2 months) history of myocardial infarction
* Recent (\< 2 months) history of stroke
* History of diabetes mellitus or impaired glucose tolerance or random blood glucose \>= 9 mMol/L
* Any acute systemic illness or infection
* Any severe disease which could interfere with survival or well-being during the study (e.g. malignancy)
* Patients of child bearing potential
* Current or previous drug and / or alcohol abuse
* Severely limited venous access
* Haemoglobin \< 10g/dL (male patients), haemoglobin \< 9g/dL (female patients)
* Requirement for anticoagulant therapy
* Severe valvular heart disease (investigator's discretion)
* Atrial fibrillation or other serious cardiac dysrhythmia
* History of thyroid disease or abnormal thyroid function test (thyroid stimulating hormone (TSH) \< 0.4 mU/L or \> 5.4 mU/L)
* History of connective tissue disorder
* Concurrent participation in any other clinical trial or participation within two months enrolment
* Requirement for restricted drugs
* Patients currently on treatment with lacidipine or bendrofluazide (BNFZ)
* Patients unable to attend clinics
* Any clinical condition which in the opinion of the investigator, would preclude the safe fulfillment of the protocol and the safe administration of trial medication
* Seated blood pressure (BP) exceeding either 210 mm Hg (systolic) or 115 mm Hg (diastolic) at screening or randomization
* Standing BP \< 140 mm Hg (systolic) and \< 95 mm Hg (diastolic) at randomization
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02235402
Study Brief:
Protocol Section:
NCT02235402