Trials / Completed
CompletedNCT02813018
The Impact of Preemptive Epidural Analgesia on Acute Postoperative Pain in Pediatric Orthopedic Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Yonsei University · Academic / Other
- Sex
- All
- Age
- 3 Years – 12 Years
- Healthy volunteers
- Not accepted
Summary
Management of postoperative pain is critical in the pediatric patients, however, safe and effective analgesia for pediatric surgical patients remains a challenge. Preemptive analgesia is based on preventing a prolonged change in central nervous system function by blocking afferent input before the surgical stimulation may evoke central sensitization and aggravate amplification and prolongation of postoperative pain. However, the clinical efficacy of preemptive analgesia is still controversial. In this study, the investigators aim to assess the impact of preemptive epidural analgesia on postoperative pain in pediatric patients for corrective osteotomy of the lower extremities expecting severe postoperative pain.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | 0.2 ml/kg of 0.2% ropivacaine | In the preemptive group, 5 minutes before skin incision, the epidural catheter is dosed with 0.2 ml/kg of 0.2% ropivacaine, followed by continuous infusion of 5 minutes before skin incision at 0.2 ml/kg/h. |
| PROCEDURE | 0.2mg/kg of Normal Saline | In the saline group, 5 minutes before skin incision, the epidural catheter is dosed with 0.2 ml/kg of normal saline, followed by continuous infusion of 5 minutes before skin incision at 0.2 ml/kg/h. |
Timeline
- Start date
- 2016-07-07
- Primary completion
- 2017-07-15
- Completion
- 2017-07-15
- First posted
- 2016-06-24
- Last updated
- 2018-06-20
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02813018. Inclusion in this directory is not an endorsement.