Perioperative Pain Management for Cleft Lip in Children
Not Applicable
- Conditions
- Perioperative Complication Pain
- Interventions
- Combination Product: i.v. analgesia
- Registration Number
- NCT04614259
- Lead Sponsor
- Cairo University
- Brief Summary
Single blind prospective randomized comparative study. 76 children between 6 months and 3 years with cleft lip will be divided in two groups. 38 children group C conventional group and 38 children group S infraorbital nerve block group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 76
Inclusion Criteria
- good physical condition.
- Age 6 months to 3 years.
- Scheduled to undergo operations for cleft lip repair. Genders eligible for study are both .
Exclusion Criteria
- Children posted for combined procedures like congenital heart correction with palatoplasty .
- Parents refusal .
- Bleeding disorders( platelets count < 100.000 , international ratio >1.5).
- Skin lesions or wounds at site of needle insertion .
- Co-morbidities as congenital heart disease , lung pathology or central nervous system
- Known hypersensitivity to local anesthetics or opioids .
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description infraorbital nerve block Bupivacain - intravenous analgesia i.v. analgesia -
- Primary Outcome Measures
Name Time Method Postoperative opioid consumption 24 huors Total rescue doses of morphine
- Secondary Outcome Measures
Name Time Method