Clinical trial · Interventional
Effect of Ultrasound-guided Erector Spinae Plane Block on Postoperative Pain and Sleep Quality of Infants With Congenital Pulmonary Cystic Disease After Thoracoscopic Surgery
NCT06498583CI-TRIAL-00109021completedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study intends to evaluate the effect of erector spinae plane block on postoperative analgesia and sleep quality in infants with congenital cystic pulmonary disease after thoracoscopic surgery, and provides reference for perioperative pain treatment in children.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bronchogenic Cyst | — | UNRESOLVED | — |
| Bronchopulmonary Sequestration | — | UNRESOLVED | — |
| Cystic Adenomatoid Malformation of Lung, Congenital | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| erector spinae plane block | Procedure | — | UNRESOLVED |
| Incision infiltration of local anesthesia | Procedure | — | UNRESOLVED |
| Ropivacaine | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- E group
- interventionNames
- Drug: Ropivacaine
- Procedure: erector spinae plane block
- type
- EXPERIMENTAL
- label
- P group
- interventionNames
- Drug: Ropivacaine
- Procedure: Incision infiltration of local anesthesia
Primary outcomes (1)
- measure
- postoperative FLACC score
- timeFrame
- 2, 4, 6, 12, 24, 48 hours after operation
Secondary outcomes (3)
- measure
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 1 Month
- Maximum age
- 12 Months
Show eligibility criteria text
Inclusion Criteria: * American Society of Anesthesiologists (ASA) status I-II * age 1 month - 12 mouths old * preoperative diagnosis was congenital cystic lung disease * thoracoscopic lung lesion resection(lung lobectomy or segmentectomy) Exclusion Criteria: * patient with a history of allergy to amide local anesthetics * family members refused to participate in the study. * combined congenital heart disease * patient with skin damage or infection at the proposed puncture site * patients with scoliosis
References
Publications (0)
Data not yet available
No reference posted for this study.