Clinical Trials Directory

Trials / Completed

CompletedNCT01172782

The Analgesic Effect of Intrathecal Hydromorphone Injection on Spinal Anesthesia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Korea University Anam Hospital · Academic / Other
Sex
All
Age
18 Years – 72 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to evaluate the adequate dose of intrathecal hydromorphone injection for postoperative pain relief after knee arthroscopic surgery.

Detailed description

Sixty patients who were undergoing unilateral knee arthroscopy randomly received unilateral spinal anesthesia with 0.5% hyperbaric bupivacaine 6 mg combined with normal saline 0.05 mL or hydromorphone 2.5, 5 or, 10 μg/0.05 mL. The verbal numerical rating scale (VNRS) pain scores were measured at 30 minutes and 2, 4, 6, 12 and 24 hours postoperatively, and the side effects of hydromorphone were recorded.

Conditions

Interventions

TypeNameDescription
DRUGHydromorphone2.5, 5, 10 ug of hydromorphone, intrathecal injection, single injection. duration of intrathecal injection are not fully studied.

Timeline

Start date
2009-07-01
Primary completion
2010-02-01
Completion
2010-07-01
First posted
2010-07-30
Last updated
2011-06-27

Source: ClinicalTrials.gov record NCT01172782. Inclusion in this directory is not an endorsement.