Clinical Trials Directory

Trials / Completed

CompletedNCT06205199

Analgesic Effect of Ropivacaine Combined With Hydromorphone for CSEA After Total Knee Arthroplasty

Analgesic Effect of Ropivacaine Hydrochloride Combined With Hydromorphone Hydrochloride for Combined Spinal-epidural Anesthesia After Total Knee Arthroplasty

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
136 (actual)
Sponsor
Second Hospital of Jilin University · Academic / Other
Sex
All
Age
55 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate the continuous analgesic effect and side effects of ropivacaine combined with hydromorphone for combined spinal-epidural anesthesia(CSEA) after total knee arthroplasty and to explore its clinical application value. To observe whether hydromorphone combined with ropivacaine can promote the rapid recovery of patients.

Detailed description

For patients undergoing total knee arthroplasty, different spinal anesthesia drugs were injected in the two groups. The spinal anesthetic drugs injected in the hydromorphone group were hydromorphone 50 μg and ropivacaine 15 mg. In the control group, the spinal anesthetic was ropivacaine 15 mg.The differences in analgesia, sedation, and side effects between the hydromorphone group and the control group were analyzed by collecting various data at different times after anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGHydromorphone was injected into the subarachnoid spaceThe dose of hydromorphone is 50 micrograms

Timeline

Start date
2022-10-27
Primary completion
2023-11-30
Completion
2023-11-30
First posted
2024-01-12
Last updated
2024-01-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06205199. Inclusion in this directory is not an endorsement.