drugset / Trial / NCT02723487
Ultrasound Guided Transversus Abdominis Plane Block in Pediatric Surgery
RandomizedParallel-groupDouble-blindPrevention
Summary
The primary objective of this study is to assess differences in postoperative pain experienced by pediatric patients having transversus abdominis plane block block with bupivacaine (0.125% and 0.25%) compared with control group will receive conventional iv analgesia after Laparoscopic surgery.
Timeline
- Start
- 2016-04
- Primary completion
- 2017-05
- Completion
- 2017-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Bupivacaine | Other / unclassified | 0.125 % | Other |
| Comparator | Bupivacaine | Other / unclassified | 0.25 % | Other |
Indications
No indication recorded.