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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02581566
Other study ID # 01003060215
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date April 2016

Study information

Verified date March 2019
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Comparison between intrathecal Dexmedetomidine versus Intraarticular Dexmedetomidine on postoperative pain after knee arthroscopy.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Adult patients, ASA I-II, undergoing knee arthroscopy under spinal anesthesia.

Exclusion Criteria:

- Absolute or relative contraindications to spinal anesthesia, allergy to dexmedetomidine or chronic pain treatment.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Intrathecal Dexmedetomidine
Addition of Intathecal Dexmedetomidine plus Intrathecal Bupivacaine
Intraarticular Dexmedetomidine
Addition of Intraarticular Dexmedetomidine plus Intrathecal Bupivacaine
Bupivacaine
Intrathecal Bupivacaine

Locations

Country Name City State
Egypt Assiut University Hospital Assiut

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain Assesment is done by Visual Analog Scale 24 hours
Secondary c-reactive protein 24 hours
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