Pain, Postoperative Clinical Trial
Official title:
Genetic, Epigenetic, Psychosocial, and Biological Determinants of Post-surgical Pain After Pectus or Spine Surgery
Verified date | January 2024 |
Source | Children's Hospital Medical Center, Cincinnati |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This will be a prospective study to determine the association between specific genotypes, epigenetics, behavioral, social and biological factors, with the phenotypes, defined by pain perception, postoperative pain, analgesic effects, side effects to perioperative analgesics, chronic postoperative pain, and gene expression in patients following pectus excavatum repair.
Status | Enrolling by invitation |
Enrollment | 600 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 8 Years and older |
Eligibility | Inclusion Criteria: - Children aged 8 years of age through adulthood - Diagnosis of pectus excavatum or adolescent idiopathic scoliosis - Scheduled for endoscopic pectus excavatum repair or spine fusion Exclusion Criteria: - History of or active renal or liver disease - Major surgery requiring opioids in the last 5 years - Severe respiratory problems (such as obstructive sleep apnea, cystic fibrosis, pulmonary fibrosis, or pneumonia within the last month) - Cardiac conditions including, but not limited to, cyanotic heart disease, hypoplastic left ventricle, arrhythmia, hypertension with ongoing treatment, Kawasaki disease, or cardiomyopathies. Participants with asymptomatic valvular lesions or defects may be included - History of seizures currently treated on medication (participants off medication and seizure free for greater than one year may be included) - Taking no more than two concomitant medications known to induce or inhibit CYP2D6 activity, including paroxetine, fluoxetine, cimetidine, and duloxetine - Needing postoperative ventilation or intraoperative cardiac bypass standby - BMI >35 - Pregnant or breastfeeding females - Non-English speaking - Definite developmental delay |
Country | Name | City | State |
---|---|---|---|
United States | Cincinnati Childrens Hospital Medical Center | Cincinnati | Ohio |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital Medical Center, Cincinnati |
United States,
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* Note: There are 204 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain score trajectory | Pain scores will be collected preoperatively through 1 year postoperatively | 1 year | |
Primary | Changes in self-reported psychosocial scores (including anxiety, pain, coping, physical limitation, etc.) | Psychosocial measures will be collected preoperatively through 1 year postoperatively | 1 year | |
Primary | Changes in heart rate variability | Heart rate variability will be assessed preoperatively and postoperatively | 8 weeks | |
Primary | Changes in mean amplitude values for lower, upper, and entire alpha frequency bands by group (intervention/no intervention) and time (pre-surgery/post-surgery) | Brain activity will be assessed preoperatively and postoperatively | 8 weeks | |
Primary | Changes in evoked response potentials (ERPs) during meditation and experimental pain tasks | Brain activity will be assessed preoperatively and postoperatively | 8 weeks | |
Primary | Changes in sleep efficiency/duration (actigraphy) and self-reported sleep quality | Sleep efficiency and quality will be assessed preoperatively and postoperatively | 8 weeks | |
Primary | Incidence of side-effect measures | Incidences of respiratory depression, sedation, postoperative nausea and vomiting will be collected during the recovery phase | 72 hours postoperatively | |
Secondary | Changes in pressure pain threshold, conditioned pain modulation, tactile discrimination, and temporal summation index | Quantitative sensory testing will be assessed preoperatively and postoperatively | 8 weeks |
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