Pediatric Postoperative Pain Clinical Trial
Official title:
Postoperative Pain After Pediatric Umbilical Hernia Repair: a Randomized Clinical Trial of Ultrasound-guided Bilateral Rectus Sheath Blocks Versus Local Anesthetic Infiltration
Verified date | September 2017 |
Source | Boston Children’s Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the use of ultrasound-guided bilateral rectus sheath blocks to local infiltration of anesthetic agent in the surgical wound in a pediatric population of patients undergoing umbilical hernia repair.
Status | Completed |
Enrollment | 53 |
Est. completion date | November 2011 |
Est. primary completion date | May 2011 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 3 Years to 12 Years |
Eligibility |
Inclusion Criteria: - Any patient who is 3 to 12 years of age - Any patient undergoing outpatient umbilical hernia repair - Any patient capable of expressing pain using the Faces Pain Rating Scale - Patient has provided assent (if age 10 or older) - Parents/guardians have provided informed consent Exclusion Criteria: - Any patient classified as ASA III, IV, or V by the American Society of Anesthesiologists - Any patient with a history of Complex Regional Pain Syndrome - Any patient with a history of chronic analgesic use - Any patient who has used an analgesic including opioids, acetaminophen, and/or NSAID's within 24 hours prior to surgery - Wards of the state - Any patient with an incarcerated umbilical hernia requiring emergent surgery - Any patient who does not speak English or Spanish - Any patient whose primary caregiver does not speak English or Spanish - Any patient who cannot express pain using the Faces Pain Rating Scale due to a disability - Any patient whose primary caregiver is unable to comply with home instructions due to a disability - Any patient less than 3 years of age or greater than 12 years of age - Any patient with renal insufficiency - Any patient with a bleeding disorder |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital Boston | Boston | Massachusetts |
United States | Children's Hospital Boston at Waltham | Waltham | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Children’s Hospital | Harvard Catalyst Pilot Grant, Harvard University |
United States,
Chan VW, Peng PW, Kaszas Z, Middleton WJ, Muni R, Anastakis DG, Graham BA. A comparative study of general anesthesia, intravenous regional anesthesia, and axillary block for outpatient hand surgery: clinical outcome and cost analysis. Anesth Analg. 2001 Nov;93(5):1181-4. — View Citation
de Jose Maria B, Götzens V, Mabrok M. Ultrasound-guided umbilical nerve block in children: a brief description of a new approach. Paediatr Anaesth. 2007 Jan;17(1):44-50. — View Citation
Jha AK, Orav EJ, Zheng J, Epstein AM. Patients' perception of hospital care in the United States. N Engl J Med. 2008 Oct 30;359(18):1921-31. doi: 10.1056/NEJMsa0804116. — View Citation
Willschke H, Bösenberg A, Marhofer P, Johnston S, Kettner SC, Wanzel O, Kapral S. Ultrasonography-guided rectus sheath block in paediatric anaesthesia--a new approach to an old technique. Br J Anaesth. 2006 Aug;97(2):244-9. Epub 2006 Jun 23. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | postoperative pain | from emergence to 24 hrs post-discharge | ||
Secondary | postoperative use of opioids and non-opioids | from emergence to 24 hrs post-discharge |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05444309 -
Ultrasound Guided Pericapsular Nerve Group Block Versus Quadratus Lumborum Block
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N/A |