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Impact of Lipoic Acid Use on Stroke Outcome After Reperfusion Therapy in Patients With Diabetes (IMPORTANT)

Primary Purpose

Stroke, Ischemic

Status
Unknown status
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
alpha lipoic acid
Saline
Sponsored by
Chonnam National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke, Ischemic focused on measuring Reperfusion, Lipoic acid, Stroke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with acute ischemic stroke within 6 hours of symptom onset
  • Patients with diabetes
  • Patients who underwent reperfusion therapy (Intravenous t-PA or endovascular thrombectomy)

Exclusion Criteria:

  • Pre-existing disability (Modified Rankin Scale >= 1)
  • Patients with severe renal disease (GFR <30 ml / min)
  • Patients whose survival period is expected to be less than 12 months due to serious diseases such as terminal cancer or liver failure

Sites / Locations

  • Chonnam National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Alpha lipoic acid

Normal saline

Arm Description

All patients will be assigned intravenous alpha lipoic acid 600mg within 24 hours of symptom onset. Patients will receive intravenous alpha lipoic acid 600mg/day for one week, followed by an oral pill of alpha lipoic acid 600mg/day for three months.

All patients will receive intravenous normal saline within 24 hours of symptom onset.

Outcomes

Primary Outcome Measures

Number of participants with functional independence
The modified Rankin Scale (mRS) consists of 7 levels, ranging from perfect health without symptoms (mRS score 0) to death (mRS score 6). We defined functional independence as mRS scores of 0-2 at 3 months after stroke.

Secondary Outcome Measures

Rate of mortality
All cause of death within 3 months
Number of participants with BBB breakdown
Hemorrhagic transformation within 1 week, Brain edema at 1 week after stroke
Number of participants with early neurological deterioration
early neurological deterioration is defined as an increase of ≥1 point in motor power or an increase of ≥2 points in the total NIHSS score within 2 weeks
Number of participants with major bleeding
Intracranial and extracranial bleeding within 3 months
Number of participants with recurrence
Recurrent stroke within 3 months

Full Information

First Posted
July 26, 2019
Last Updated
July 31, 2019
Sponsor
Chonnam National University Hospital
Collaborators
Chosun University Hospital, Chonbuk National University Hospital, Wonkwang University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04041167
Brief Title
Impact of Lipoic Acid Use on Stroke Outcome After Reperfusion Therapy in Patients With Diabetes (IMPORTANT)
Official Title
Impact of Lipoic Acid Use on Stroke Outcome After Reperfusion Therapy in Patients With Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
July 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chonnam National University Hospital
Collaborators
Chosun University Hospital, Chonbuk National University Hospital, Wonkwang University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study aims to investigate the effectiveness and safety of alpha-lipoic acid in patients with diabetes and ischemic stroke treated with reperfusion therapy.
Detailed Description
Despite significant advances in the prevention and treatment of stroke, it is still one of the leading causes of death and debilitating disease. Unfortunately, several neuroprotective strategies have failed in clinical trials. At present, it is reported that there are no pharmacological agents with putative neuroprotective actions that have demonstrated efficacy in improving outcomes after acute ischemic stroke (AIS) in humans. Previous stroke studies have confirmed that oxidative stress plays a vital role in stroke and in reperfusion following stroke. Therefore, the use of antioxidants could be a promising strategy for treating ischemia-reperfusion injury. Alpha-lipoic acid (aLA) is a potent antioxidant commonly used for the treatment of diabetic polyneuropathy (DPNP). The investigators previously demonstrated the neuroprotective and neurorestorative effects of aLA, mediated at least partially via insulin receptor activation, after cerebral ischemia in rats. Moreover, previous observational study of the investigators showed that patients with diabetes treated with aLA have better functional outcomes following AIS after reperfusion therapy than patients not using aLA. Therefore, the investigators investigate whether patients with diabetes treated with aLA have better functional outcomes after AIS and reperfusion therapy than patients not treated with aLA in this prospective randomized trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Ischemic
Keywords
Reperfusion, Lipoic acid, Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alpha lipoic acid
Arm Type
Active Comparator
Arm Description
All patients will be assigned intravenous alpha lipoic acid 600mg within 24 hours of symptom onset. Patients will receive intravenous alpha lipoic acid 600mg/day for one week, followed by an oral pill of alpha lipoic acid 600mg/day for three months.
Arm Title
Normal saline
Arm Type
Placebo Comparator
Arm Description
All patients will receive intravenous normal saline within 24 hours of symptom onset.
Intervention Type
Drug
Intervention Name(s)
alpha lipoic acid
Other Intervention Name(s)
thioctacid
Intervention Description
alpha lipoic acid treatment
Intervention Type
Drug
Intervention Name(s)
Saline
Other Intervention Name(s)
normal saline
Intervention Description
No alpha lipoic acid treatment
Primary Outcome Measure Information:
Title
Number of participants with functional independence
Description
The modified Rankin Scale (mRS) consists of 7 levels, ranging from perfect health without symptoms (mRS score 0) to death (mRS score 6). We defined functional independence as mRS scores of 0-2 at 3 months after stroke.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Rate of mortality
Description
All cause of death within 3 months
Time Frame
3 months
Title
Number of participants with BBB breakdown
Description
Hemorrhagic transformation within 1 week, Brain edema at 1 week after stroke
Time Frame
1 week
Title
Number of participants with early neurological deterioration
Description
early neurological deterioration is defined as an increase of ≥1 point in motor power or an increase of ≥2 points in the total NIHSS score within 2 weeks
Time Frame
2 weeks
Title
Number of participants with major bleeding
Description
Intracranial and extracranial bleeding within 3 months
Time Frame
3 months
Title
Number of participants with recurrence
Description
Recurrent stroke within 3 months
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with acute ischemic stroke within 6 hours of symptom onset Patients with diabetes Patients who underwent reperfusion therapy (Intravenous t-PA or endovascular thrombectomy) Exclusion Criteria: Pre-existing disability (Modified Rankin Scale >= 1) Patients with severe renal disease (GFR <30 ml / min) Patients whose survival period is expected to be less than 12 months due to serious diseases such as terminal cancer or liver failure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kangho Choi, MD, PhD
Phone
82-62-220-6137
Email
ckhchoikang@hanmail.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kangho Choi, MD, PhD
Organizational Affiliation
Chonnam National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chonnam National University Hospital
City
Gwangju
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kangho Choi, MD, PhD
Phone
82-62-220-6137
Email
ckhchoikang@hanmail.net

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
IPD will be shared with other researchers.
IPD Sharing Time Frame
We will share the data for one year after the end of the study.
IPD Sharing Access Criteria
If a proposal for a joint research or a sub-study is proposed, the approval will be decided through a meeting of the committee.
Citations:
PubMed Identifier
27677185
Citation
Choi KH, Park MS, Kim JT, Kim HS, Kim JH, Nam TS, Choi SM, Lee SH, Kim BC, Kim MK, Cho KH. Lipoic Acid Use and Functional Outcomes after Thrombolysis in Patients with Acute Ischemic Stroke and Diabetes. PLoS One. 2016 Sep 27;11(9):e0163484. doi: 10.1371/journal.pone.0163484. eCollection 2016.
Results Reference
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PubMed Identifier
25761600
Citation
Choi KH, Park MS, Kim HS, Kim KT, Kim HS, Kim JT, Kim BC, Kim MK, Park JT, Cho KH. Alpha-lipoic acid treatment is neurorestorative and promotes functional recovery after stroke in rats. Mol Brain. 2015 Feb 11;8:9. doi: 10.1186/s13041-015-0101-6.
Results Reference
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Impact of Lipoic Acid Use on Stroke Outcome After Reperfusion Therapy in Patients With Diabetes (IMPORTANT)

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