Skip to content

PROspective Study to OPTimize thE HEALTH of Patients With TIAs (Transient Ischemic Attacks) and Stroke Admitted to the Hamad General Hospital

PROspective Study to OPTimize thE HEALTH of Patients With TIAS (Transient Ischemic Attack) and Stroke Admitted to the Hamad General Hospital

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02868723
Acronym
PROMOTE-HEALTH
Enrollment
400
Registered
2016-08-16
Start date
2017-11-12
Completion date
2019-12-30
Last updated
2018-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Transient Ischemic Attack (TIA)

Keywords

cerebrovascular disease, patient management, stroke management, prognosis, 3D Carotid Doppler Imaging, Randomization

Brief summary

This will be a prospective randomized 2 year study of patients admitted to the Hamad General Hospital (HGH) and the Stroke Prevention Clinic with a diagnosis of ischemic stroke (IS) and Transit ischemic attacks (TIAs). After signing of the informed consent forms and initial evaluation and investigations, all patients enrolled in the two arms ( study arm and control arm) of the study will be followed for one year (monthly visits for the first three months followed by visits three months until completion of study: total of 6 follow up visits) and the pre-specified investigations repeated at the one year follow up. In one arm (the control group), the patients will be offered best risk factor management strategies as currently being practiced by stroke specialists at HGH in Qatar. And in the second ( the subject group) arm, with assistance of a nurse-practitioner and pharmacist, the investigators will make aggressive attempts to meet to target defined risk factors and have the evaluations and investigations completed as in the initial year cohort. All patients will have risk factor stratification according the Framingham Risk Score (FRS) and the change in score measured over time.The primary objective will be to determine if an approach that utilizes a comprehensive strategy results in a significantly outcome. A clinically 'meaningful' difference in the blood pressure (BP) and lipid control of 10% between the aggressively managed versus patients treated with the standard of care will require minimum of 200 patients in each group (alpha error set at 0.05 and beta error at 0.20, power 80%) to be recruited over 1 year and followed for one year (total study duration 2 years). All patients will have screening magnetic resonance imaging (MRI) (including gradient echo (GRE) sequence), carotid 3D Doppler measurement of plaque volume, and PAD assessments, C-reactive protein (CRP) and evaluation for protein urea at baseline. These studies will be repeated in 1 year at the time of exit from the study. The co-primary objective would be to monitor progression (or regression) of plaque build-up on 3D Doppler imaging of the carotid arteries between the two cohorts. The investigators hypothesize that aggressive management of vascular risk factors to recommended target levels will lead to better vascular health. Compared to current practice, comprehensive and coordinated approach at preventive measures will lead to more patients with better control of blood pressure and lipid levels. Improved risk factor management will result in slowing of atherosclerosis and its downstream effects which will be measurable on sophisticated blood and imaging testing. Clinically this will translate into fewer hospital re-admissions.

Interventions

OTHERAggressive Management

With the aid of the nurse and pharmacist, the individuals in the interventional group will receive additional management of stroke by change is diet plan, increased exercise

Sponsors

Hamad Medical Corporation
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* ISCHEMIC STROKE OR TIA including ocular stroke such as Amaurosis Fugax, within the past year (not intracranial hemorrhage or due to trauma, malignancy or cardio-embolic related to structural heart disease) * MEETS AT LEAST ONE OF THE FOLLOWING THREE CRITERIA: * systolic Bp\>140 mmHg but \<200 mmHg (at 24 HR from admission/if clinic visit 3 readings 5 minutes apart) * fasting LDL cholestrol \>2.0 (MEASURED WITHIN PREVIOUS 6 MONTH) * total: HDL cholestrol ratio \>4.0 (measured within previous 6 month) * Willing to participate (by signing consent form)and willing to return for study-related scheduled follow up visits for one year from the time of enrollment into the study

Exclusion criteria

* Participation in concurrent interventional trial related to stroke or vascular disease * Any condition, including foreshortened life-expectancy or severe comorbidities that would preclude treatment benefit or 12-month follow up. * Institutionalized in a long term care facility * Already on maximal therapy for risk factors: * On 3 ANTI HTN drugs at maximal dose (if htn is inclusion criteria) * On maximal dose of statin (if elevated LDL-cholesterol is inclusion criteria) * CT or MRI shows evidence of primary intracranial hemorrhage or neoplasm * Active coronary artery disease * Severe Renal on hemo-dialysis(HD) or Severe Hepatic dysfunction * Cognitive dysfunction severe enough to interfere with patients ability to give informed consent * Severe systemic illness that will not allow for the patient to complete the one year trial * History of intolerance to statins or commonly used anti-hypertensive medications(intolerance/contraindication to statin(if elevated LDL-c is the inclusion criteria) * Unable to tolerate antiplatelet agents * Decline of consent * Reside outside Qatar * Unable to participate (due cognition, mobility, language barrier)

Design outcomes

Primary

MeasureTime frameDescription
Progression/regression of 3D plaque volumeone year3D carotid doppler imaging studies

Secondary

MeasureTime frameDescription
Measurement of blood pressureone yearmanagement of life style
Measurement of Lipid levelsone yearmanagement of lifestyle

Countries

Qatar

Contacts

Primary ContactYAHIA Z BASHIER IMAM, MBBS,MD,MRCP,MRCPE
yimam@hamad.qa55246887
Backup ContactNIMA K EL KHAWAD MOHAMED AHMED, MBBS
drnima88@gmail.com33141880

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026