Ureteropelvic Junction Obstruction Clinical Trial
Official title:
Pediatric Robotic Versus Open Pyeloplasty: A Pilot Randomized Control Study
Verified date | May 2024 |
Source | Indiana University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective is conduct a pilot randomized controlled trial comparing robotic and open techniques for surgical correction of congenital UPJ obstruction (pyeloplasty) in pediatric patients. This study will serve as a proof of concept trial to demonstrate feasibility of recruiting pediatric patients to participate in a randomized study for surgical procedures and delineate patient-centered outcomes. Should this study prove randomization is feasible, a randomized comparative effectiveness trial with sufficient power to determine whether open or robotic-assisted pyeloplasty has superior patient-centered outcomes will be pursued.
Status | Terminated |
Enrollment | 11 |
Est. completion date | June 23, 2021 |
Est. primary completion date | November 14, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 2 Years to 8 Years |
Eligibility | For Aim 2: Inclusion Criteria: - Primary UPJ obstruction diagnosed by scan and presenting to the pediatric urology clinic for evaluation - Patient between age 2 - 8 years old Exclusion Criteria: - Serious comorbidities (cardiovascular or respiratory disease, or other congenital anomalies requiring surgical intervention). - BMI greater than the 95th %tile for age. |
Country | Name | City | State |
---|---|---|---|
United States | Riley Children's Hospital | Indianapolis | Indiana |
Lead Sponsor | Collaborator |
---|---|
Indiana University | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
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* Note: There are 52 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Length of Post Op Inpatient Hospital Stay Measured in Days | Number of inpatient hospital days post surgery obtained via retrospective chart. | surgery to discharge | |
Primary | Number of Doses of Narcotic Pain Medication In the First 24 Hours Post Op | Pain medication use during hospitalization obtained via retrospective chart review. Dose recorded in mg and frequency recorded as number of doses administered in 24 hour period | Surgery to the first 24 hours post op | |
Primary | Total Dose of Narcotic Pain Medication In the First 24 Hours Post Op in Morphine Milligram Equivalents (MME) | Pain medication use during hospitalization obtained via retrospective chart review. Morphine milligram equivalents (MME) are values that represent the potency of an opioid dose relative to morphine | Surgery to the first 24 hours post op | |
Primary | Grade of Surgical Complications up to 1 Year Post op Using Clavian-Dindo Classification | This s a standardized scale to rank the severity of a surgical complication. The higher the grade the more severe the surgical complication. Minimum value is Grade "0" no complication to maximum Grade IV life threatening complication. Grades I thru IV defined as:
Grade I Any deviation from the normal postoperative course without the need for pharmacological treatment or surgical, endoscopic and radiological interventions. This grade also includes wound infections opened at the bedside ; Grade II Requiring pharmacological treatment with drugs other than such allowed for grade I complications. Blood transfusionsand total parenteral nutritionare also included; Grade III Requiring surgical, endoscopic or radiological intervention; Grade IV Life-threatening complication (including CNS complications)* requiring IC/ICU-management |
up to 1 year post up | |
Primary | Pain Score Measured Using The FLACC at 2 Week Post Op Follow Up | Obtained from hospital record and participant report post discharge via the FLACC (behavioral scale for scoring postoperative pain in young children). FLACC score range: minimum "0" ( comfortable) and "10" (severe discomfort) | 1 week post op follow up | |
Primary | Length Of Time For Patient To Return To Normal Routine After Surgery Measured in Days at 2 Week Post Follow Up | Study team created a questionnaire to better understand patient's post op experience. Participant to complete questionnaire with targeted questions on: Side effects of medication and impact; Experience of having a temporary ureteral stent; Ease of removing stent; Return to activity; Financial burden reported by family. No scale or scoring utilized to assess outcome. | 2 week post op follow up | |
Primary | Length Of Time Parent Was Out Of Work After Child's Surgery Measured in Days at 2 Week Post Follow Up | Number of days parent out of work after operation obtained by parent report. No scale or scoring utilized to assess outcome.
Participant asked "Have you returned to work since your child's surgery?". If "Yes", asked to estimate the length of time you were out of work after your child's operation. |
2 week post op follow up | |
Primary | Satisfaction With Scar Appearance Measured Using the Patient Scar Assessment Questionnaire at 3 Month Follow Up Visit | Participant completed the Patient Scar Assessment Questionnaire (PSAQ) at 3 month follow up visit. The 3 month follow up was scheduled at the 6 week post op visit. The "Satisfaction with Appearance" subscale consists of a 8 items with 4-point categorical responses, scoring 1 to 4 points (with 1 point assigned to the most favourable category and 4 assigned to the least favourable). The minimum score of this scale is an "8" and maximum "32." | up to 3 month follow up visit (18 weeks post op) | |
Primary | Satisfaction With Symptoms Measured Using the Patient Scar Assessment Questionnaire at 3 Month Follow Up Visit | The Patient Scar Assessment Questionnaire (PSAQ) was completed at the 3 month follow up (scheduled at the 6 week post op visit).
Higher scores reflect a poorer perception of the scar related to the domain being evaluated. The "Satisfaction with Symptoms" subscale consists of a 5 items with 4-point categorical responses, scoring 1 to 4 points (with 1 point assigned to the most favourable category and 4 assigned to the least favourable). The minimum score of this scale is an "5" and maximum "20. |
up to 3 month follow up visit (18 weeks post op) | |
Primary | Quality of Life Measured Using The Glasgow Children's Benefit Inventory at 3 Month Follow Up Visit | Participant completed the GCBI at 3 month follow up visit. The 3 month follow up was scheduled at the 6 week post op visit.
The Glasgow Children's Benefit Inventory (GCBI). is a 24 question 5 point Likert scale 2 (much better) to -2 (much worse) with scoring range from -100 (maximum harm) to +100 (maximum benefit). |
3 month follow up visit |
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