Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
PHASE4
64 participants
INTERVENTIONAL
2025-03-10
2026-04-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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IV Magnesium Sulfate adjuvant group
Participants in this group will receive standard-of-care procedures intraoperatively and postoperatively along with IV magnesium sulfate for pain control.
IV Magnesium Sulfate
Participants will receive IV Magnesium Sulfate intraoperatively.
Control group
Participants in this group will receive standard-of-care procedures intraoperatively and post-operatively for pain control.
No interventions assigned to this group
Interventions
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IV Magnesium Sulfate
Participants will receive IV Magnesium Sulfate intraoperatively.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* patients with 2nd or 3rd degree AV block
* patients with severe renal insufficiency
* patients with heart failure
* patients with bradycardia
14 Years
89 Years
ALL
No
Sponsors
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University Hospitals Cleveland Medical Center
OTHER
Responsible Party
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Robert Wetzel, MD
Orthopedic Trauma Surgeon
Principal Investigators
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Robert Wetzel, MD
Role: PRINCIPAL_INVESTIGATOR
University Hospitals
Locations
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University Hospitals
Cleveland, Ohio, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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STUDY20230720
Identifier Type: -
Identifier Source: org_study_id
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