Trials / Completed
CompletedNCT05063461
Evaluation of the Analgesia Nociception Index With Varying Remifentanil Concentrations Under Sevoflurane
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Beijing Chao Yang Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
Analgesia Nociception Index(ANI)which is derived from heart rate variability can be used to detect noxious stimulation during propofol while changing remifentanil concentrations. The aim of this study is to verify the effectiveness of ANI predictability for actual surgical noxious stimuli while satisfying the individual analgesic status by pre-tetanus-induced ANI determination during sevoflurane while changing remifentanil concentrations.
Detailed description
General anesthesia with sevoflurane and remifentanil is widely used in minor surgeries. Monitoring noxious stimulation during general anesthesia is still worth further studies and reaching clinical consensus. Analgesia Nociception Index can be used to detect noxious stimulation during propofol while changing remifentanil concentrations. Previous studies suggest that an ANI≥50 can be useful in detecting sufficient analgesia for patients who cannot self-report pain. The aim of this study is to verify the effectiveness of ANI predictability for actual surgical noxious stimuli while satisfying the individual analgesic status by pre-tetanus-induced ANI determination during sevoflurane while changing remifentanil concentrations.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Tetanic stimulation | For each participant, record the first concentration that ANI≥50 after the tetanic stimuli, as the sufficient concentration. |
| PROCEDURE | Skin incision | Infuse the sufficient concentration for at least 5min of the steady-state period, then surgical stimulus is applied. The surgical stimulus is defined as the first skin incision to establish pneumoperitoneum. |
Timeline
- Start date
- 2021-09-25
- Primary completion
- 2023-02-28
- Completion
- 2023-03-01
- First posted
- 2021-10-01
- Last updated
- 2023-03-22
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05063461. Inclusion in this directory is not an endorsement.