Intra-Articular Dexmedetomidine: A Treatment for Chronic Knee Pain
NCT ID: NCT06641206
Last Updated: 2024-10-15
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
NA
70 participants
INTERVENTIONAL
2024-09-17
2025-03-31
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
TREATMENT
DOUBLE
Study Groups
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Group 1
A group of Patients from Tanta University suffering from Chronic painful knee osteoarthritis who didn't receive medical treatment and progressed to have chronic pain with decreased physical function and poorer quality of life.
Triamcinolone Acetonide
1 ml of triamcinolone acetonide was used to prepare a solution for knee injection for patients with Chronic Knee Pain
Bupivacaine Hydrochloride
20mg of bupivacaine hydrochloride was used to prepare a solution for knee injection for patients with Chronic Knee Pain
Group 2
A group of Patients from Tanta University suffering from Chronic painful knee osteoarthritis who didn't receive medical treatment and progressed to have chronic pain with decreased physical function and poorer quality of life.
Dexmedetomidine
Dexmedetomidine solution was prepared by mixing Dexmedetomidine in a dose of 3 µg/kg in 5-ml saline
Interventions
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Triamcinolone Acetonide
1 ml of triamcinolone acetonide was used to prepare a solution for knee injection for patients with Chronic Knee Pain
Bupivacaine Hydrochloride
20mg of bupivacaine hydrochloride was used to prepare a solution for knee injection for patients with Chronic Knee Pain
Dexmedetomidine
Dexmedetomidine solution was prepared by mixing Dexmedetomidine in a dose of 3 µg/kg in 5-ml saline
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients who had uncontrolled hypertension and/or diabetes mellitus;
* Patients who had uncompensated cardiac, renal, or hepatic diseases;
* Patients with coagulopathy, spinal deformity, allergy, or contraindication for the used drugs;
* Patients who refused to sign the informed consent were excluded from the study.
40 Years
75 Years
ALL
No
Sponsors
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Tanta University
OTHER
Responsible Party
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Ahmed ElKashef
lecturer of Anesthesia and Surgical ICU, Faculty of Medicine
Locations
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Tanta University
Tanta, El Gharbyia, Egypt
Countries
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Facility Contacts
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Other Identifiers
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36264PR843/9/24
Identifier Type: -
Identifier Source: org_study_id
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