NCT06702787

Brief Summary

The MEMENTO (MEchanical thrMobectomy NETwork for MENA TOgether) Registry is a multicenter, prospective observational study aiming to evaluate the effectiveness, safety, and cost-effectiveness of mechanical thrombectomy (MT) in patients with acute ischemic stroke (AIS) due to large vessel occlusions (LVO) in the Middle East and North Africa (MENA) region. This interim analysis reports on the first 499 patients enrolled, assessing clinical outcomes, procedural details, and economic implications.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 11, 2022

Completed
2.7 years until next milestone

First Submitted

Initial submission to the registry

November 14, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

November 25, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 11, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 11, 2025

Completed
Last Updated

November 25, 2024

Status Verified

November 1, 2024

Enrollment Period

3.1 years

First QC Date

November 14, 2024

Last Update Submit

November 22, 2024

Conditions

Keywords

Mechanical ThrombectomyAcute IschemicStroke Large Vessel OcclusionMiddle East and North Africa MENA RegionEndovascular TreatmentCerebral InfarctionBrain IschemiaStroke ManagementReperfusion TherapyNeurointervention Cerebrovascular

Outcome Measures

Primary Outcomes (1)

  • Functional Independence at 90 Days

    Description: Proportion of patients achieving a modified Rankin Scale (mRS) score of 0-2 at 90 days post-procedure.

    90 days post-procedure

Secondary Outcomes (6)

  • Proportion of Patients Achieving TICI Score ≥2b After MT

    Immediately post-procedure

  • Improvement in NIHSS Score from Baseline to 24 Hours and at Follow-up

    Baseline, 24 hours, and up to 90 days

  • Symptomatic Intracerebral Hemorrhage (sICH) Rate

    Within 7 days post-procedure

  • All-Cause Mortality at 90 Days

    90 days post-procedure

  • Complication Rate

    Immediately post-procedure up to 7 days

  • +1 more secondary outcomes

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Consecutive patients presenting with acute ischemic stroke due to LVO or MeVO at participating centers in the MENA region, who received MT as part of standard clinical practice.

You may qualify if:

  • Adults aged 18 years and older (no upper age limit). Diagnosed with acute ischemic stroke due to confirmed large vessel occlusion (LVO) or medium vessel occlusion (MeVO).
  • Underwent mechanical thrombectomy (MT) with or without prior intravenous thrombolysis (IV tPA).
  • Pre-stroke modified Rankin Scale (mRS) score of 0-5. Consent to participate in the registry (by patient or legal representative).

You may not qualify if:

  • Absence of confirmed LVO or MeVO. Pre-stroke mRS score of 6. Known severe comorbid conditions precluding MT. Inability to obtain informed consent. Patients not treated with MT.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Alexandria University Stroke network

Alexandria, Alexandria Governorate, Egypt

Location

MeSH Terms

Conditions

StrokeCerebral InfarctionBrain Ischemia

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesBrain InfarctionInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • ossama yassin MANSOUR, MD, PhD,

    Alexandria University

    PRINCIPAL INVESTIGATOR
  • farouk Hassan, MD,Phd

    cairo university, Egypt

    PRINCIPAL INVESTIGATOR
  • Atila Oscan Ozdimar, MD, PhD

    Eskisehir Osmangazi University

    PRINCIPAL INVESTIGATOR
  • Syed Irteza Hussain, MD

    Cleveland Clinic Abu Dhabi

    PRINCIPAL INVESTIGATOR
  • Faisal Alghamdi, MD

    King Abdullah Medical City

    PRINCIPAL INVESTIGATOR
  • Nadia Hammami, MD

    institut National de Neurologie

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
90 Days
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 14, 2024

First Posted

November 25, 2024

Study Start

March 11, 2022

Primary Completion

April 11, 2025

Study Completion

September 11, 2025

Last Updated

November 25, 2024

Record last verified: 2024-11

Locations