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OpenTrials
Completed

NCT Number: NCT03036631

Ideal Sedation for Stroke Thrombectomy

The Ideal Sedation for Stroke Thrombectomy (ISST) registry will answer the key questions whether sedation with intubation and paralytics is feasible and whether it delays the time to recanalization in comparison with conscious sedation alone. As a pilot registry, it is anticipated to enroll 40 acute stroke patients requiring mechanical thrombectomy over 12-18 months. Following enrollment, data will be collected prospectively from medical records and from patients' visits.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Los Robles Hospital and Medical Center

Thousand Oaks, California, 91360, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Suitable for intra-arterial treatment for acute stroke up to 8 hours from onset of symptoms
  • Clinical equipoise for best mode of sedation

Exclusion criteria

  • Any known allergy to either proposed medication and its alternative
  • Any patient that has been intubated prior to randomization
  • Posterior circulation strokes
  • Age ≤ 18
  • Pregnant female

Treatment and study plan

Primary outcomes

  1. Time interval between groin puncture and final recanalization

    Time frame: 6 months or at study completion

Sponsors and collaborators

Lead sponsor

Dr. M. Asif Taqi

Other

Registry information

Acronym: ISST

Important dates

Study start
2016
Primary completion
2018
Study completion
2018
First posted
Jan 30, 2017
Registry last updated
Jul 19, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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