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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NOT_YET_RECRUITING
PHASE4
126 participants
INTERVENTIONAL
2026-02-01
2028-06-30
Brief Summary
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Patients will be randomized to either receive standard anesthesia with OR without ketamine. The surgical procedure will be the same regardless of which group patients are randomized to. After surgery, patients will be asked to rate their pain in the post-operative observation unit and at their two-week post-operative visit. No additional visits are required for participation in this study. The investigators estimate the surveys will take approximately 10 minutes to complete.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Control
standard general anesthesia without ketamine
No interventions assigned to this group
Ketamine
standard general anesthesia with ketamine
ketamine
Participants will receive general anesthesia with protocoled ketamine infusion
Interventions
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ketamine
Participants will receive general anesthesia with protocoled ketamine infusion
Eligibility Criteria
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Inclusion Criteria
* ASA classification I-III
* outpatient elective laparoscopy for endometriosis
Exclusion Criteria
* History of substance use disorder, including alcohol or marijuana use, both current and remote
* History of severe psychiatric illness, including schizoaffective disorder, bipolar disorder, psychosis, or decompensated psychiatric condition , excluding anxiety and depression
* Current Intraoperative complications
18 Years
89 Years
FEMALE
No
Sponsors
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University Hospitals Cleveland Medical Center
OTHER
Responsible Party
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Adi Cosic
Physician
Principal Investigators
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Adi Cosic, DO
Role: PRINCIPAL_INVESTIGATOR
University Hospitals
Morgan Cheeks, MD
Role: PRINCIPAL_INVESTIGATOR
University Hosptials
Locations
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University Hospitals Cleveland Medical Center
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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STUDY20250700
Identifier Type: -
Identifier Source: org_study_id
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