Using Real-world Evidence to Analyze the Clinical Effects and Adverse Events of Butylphthalide in Stroke Patients

Sponsor
Xin Huang (Other)
Overall Status
Recruiting
CT.gov ID
NCT05086874
Collaborator
(none)
10,000
1
42.8
233.4

Study Details

Study Description

Brief Summary

This is a retrospective, multi-center, real-world study. The researchers plan to include 10,000 cases of ischemic stroke patients using butylphthalide and 10,000 cases of ischemic stroke patients using Urinary Kallidinogenase. The main purpose is to analyze the effectiveness and safety of butylphthalide and establish the drug risk assessment management plan.

Detailed Description

Ischemic stroke is a type of syndrome in which blood supply to the brain is impaired due to various reasons, leading to local brain tissue ischemia, hypoxic necrosis, and corresponding neurological deficits. It has a high incidence, high morbidity and disability. Features of high recurrence rate.

Butylphthalide can improve the damage of central nervous system in patients with acute ischemic stroke, and can promote the improvement of patients with neurological deficits. Regarding butylphthalide in the treatment of ischemic stroke, there is still a lack of big data research based on the efficacy and safety of the real world.

Therefore, it is planned to include 10,000 patients who used butylphthalide or Urinary Kallidinogenase in five hospitals from 2019 to 2021, and record the basic information of the patients, medication status and related test results. The data was cleaned, sorted and analyzed to evaluate the effectiveness and safety of butylphthalide in the treatment of ischemic stroke.

Study Design

Study Type:
Observational
Anticipated Enrollment :
10000 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Real-world Retrospective Study on the Effectiveness and Safety of Butylphthalide in the Treatment of Ischemic Stroke
Actual Study Start Date :
May 7, 2022
Anticipated Primary Completion Date :
Sep 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Exposed group

A group of patients with ischemic stroke, treated with butylphthalide

Other: butylphthalide
Observational only and no predesigned interventions in this study
Other Names:
  • observational only ,no intervention
  • Non-exposed group

    A group of patients with ischemic stroke, treated with Urinary Kallidinogenase

    Outcome Measures

    Primary Outcome Measures

    1. The incidence of adverse events [90days]

      The probability of unanticipated and adverse medical events after the patient receives medication, but it does not necessarily have a causal relationship with the treatment

    Secondary Outcome Measures

    1. NIHSS [90days]

      NIH stroke scale (NIHSS) to assess the degree of neurological deficit in stroke patients. The score ranges from 0 to 42 points, the higher the score, the more severe the nerve damage. Patients with a baseline assessment of> 16 points are likely to die, while those with a score of <6 are likely to recover well; for each additional point, the probability of a good prognosis is reduced by 17%

    2. mRS [90days]

      Modified Rankin scale (mRS) is an indicator of the efficacy of functional disability. The score ranges from 0 to 5 points, and the clinical score will be increased to 6 points to indicate death. The higher the score, the more disability the patient is.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • From January 2019 to August 2021, clinicians diagnosed patients with ischemic stroke requiring hospitalization.
    Exclusion Criteria:
    • Patients who are unable to obtain information such as medical advice, laboratory test results, etc.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Shandong Provincial Qianfoshan Hospital Jinan Shandong Provincial China 250014

    Sponsors and Collaborators

    • Xin Huang

    Investigators

    • Study Director: Xin Huang, Qianfoshan Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Xin Huang, Chief Pharmacist, Qianfoshan Hospital
    ClinicalTrials.gov Identifier:
    NCT05086874
    Other Study ID Numbers:
    • QFS-HX-2021-DBT-HGX-001
    First Posted:
    Oct 21, 2021
    Last Update Posted:
    May 10, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Xin Huang, Chief Pharmacist, Qianfoshan Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 10, 2022