Clinical Trials Directory

Trials / Completed

CompletedNCT04387097

Drip-infusion of Remifentanil for RIH

Postoperative Drip-infusion of Remifentanil for Preventing Remifentanil-induced Hyperalgesia- a Retrospective Observative Study

Status
Completed
Phase
Study type
Observational
Enrollment
559 (actual)
Sponsor
Tri-Service General Hospital · Academic / Other
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The development of remifentanil-induced hyperalgesia (RIH) is an unpleasant experience for surgical patients. An alternative management, gradual withdrawal of remifentanil was effective in prevention of RIH. The investigators designed a simple modality to assess if under withdrawal of remifentanil and further drip-infusion of remifentanil immediately after extubation affected postoperative pain score, the requirement of rescue analgesics, and adverse effects.

Detailed description

In clinical practice, the gradual withdrawal of remifentanil during surgery is unsatisfied. Thus, the investigators conducted a simple modality in a single center retrospective cohort study to assess how under baseline gradual withdrawal of remifentanil and further drip infusion of remifentanil immediately after extubation affected postoperative pain score and use of analgesics.

Conditions

Interventions

TypeNameDescription
DRUGremifentanilpostoperative drip-infusion of remifentanil

Timeline

Start date
2018-05-01
Primary completion
2019-01-31
Completion
2019-07-22
First posted
2020-05-13
Last updated
2020-05-15

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT04387097. Inclusion in this directory is not an endorsement.