Trials / Withdrawn
WithdrawnNCT02683837
Pupillometry Guided Remifentanil Administration In Pediatric Anesthesia
A Prospective Randomized Study Evaluating Pupillometry Guided Remifentanil Administration in Pediatric Anesthesia
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- University Hospital, Geneva · Academic / Other
- Sex
- All
- Age
- 2 Years – 16 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this prospective randomized study is to evaluate the impact of peroperative pupillometry monitoring on per and post-operative opioid consumption in pediatric anesthesia. All patients are anesthetized with sevoflurane and remifentanil. In the intervention group, peroperative remifentanil infusion rate is guided by pupillometry. In the other group, remifentanil infusion rate is guided according to hemodynamic data.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Remifentanil | |
| DEVICE | Pupillometry | Pupillary diameter measured every 5 minutes |
| DRUG | Sevoflurane | Administered to maintain a Bispectral Index between 40 and 60 |
Timeline
- Start date
- 2016-04-01
- Primary completion
- 2016-11-01
- Completion
- 2022-12-01
- First posted
- 2016-02-17
- Last updated
- 2024-04-18
Locations
1 site across 1 country: Switzerland
Source: ClinicalTrials.gov record NCT02683837. Inclusion in this directory is not an endorsement.