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
| Type | Name | Description |
|---|---|---|
| DRUG | remifentanil | postoperative 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.