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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04467463
Other study ID # N-98-2019
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2020
Est. completion date December 2020

Study information

Verified date June 2020
Source Cairo University
Contact Sherif Abdullah Mohamed, M.D.
Phone +201002013497
Email dr.sherif213@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Regional blocks are commonly used in pediatric anesthesia to achieve adequate postoperative analgesia. Suprazygomatic Maxillary nerve block (SMN) and Greater Palatine nerve block (GPN) are regional blocks described for use during cleft palate (CP) repair surgery.The aim of this study was to compare the analgesic effect as well as the incidence of complications associated with the use of bilateral GPN and bilateral SMN blocks in children undergoing palatoplasty surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group 6 Months to 5 Years
Eligibility Inclusion Criteria: - ASA I-III scheduled to undergo palatoplasty Exclusion Criteria: - bleeding disorders, - skin lesions or wounds at site of proposed needle insertion, - congenital heart disease, - respiratory or - cardiovascular disorders, - children scheduled for combined procedures like palatoplasty with cheiloplasty or submucosal alveolar bone grafting, - known hypersensitivity to local anesthetics or opioids and - lack of parental consent.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
peripheral nerve block by 0.25% levobupivacaine
SUBMANDIBULAR nerve block will be performed using a 25G 90 mm beveled needle . the entry point of the needle will be situated at the angle formed by the superior edge of the zygomatic arch below and the posterior orbital rim forward .The needle will be inserted perpendicular to the skin and advanced approximately 20 mm depth to reach the greater wing of the sphenoid deep to the pterygopalatine fossa. Injection of 1ml of 0.25% levobupivacaine will be done over 20 seconds afterensuring negative blood aspiration .greater Palatine Nerve will be blocked bilaterally as it leaves on palatal side through the foramen on the opposite direction of the anterior part of the 3rd molar orthe posterior part of the 2nd molar tooth.

Locations

Country Name City State
Egypt anesthesia department at Cairo University Cairo
Egypt Cairo University hospitals Cairo Manial

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

References & Publications (4)

3. Tremlett M. Anaesthesia for cleft lip and palate surgery. Curr Anaesth Crit Care. 2004;15:309-16.

Diewert VM. Development of human craniofacial morphology during the late embryonic and early fetal periods. Am J Orthod. 1985 Jul;88(1):64-76. — View Citation

Lee SJ, Ralston HJ, Drey EA, Partridge JC, Rosen MA. Fetal pain: a systematic multidisciplinary review of the evidence. JAMA. 2005 Aug 24;294(8):947-54. Review. — View Citation

Pain terms: a list with definitions and notes on usage. Recommended by the IASP Subcommittee on Taxonomy. Pain. 1979 Jun;6(3):249. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain score Pain assessment was done immediately postoperative using Objective behavioral pain score the first 12 postoperative hours
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