Chronic Postsurgical Pain

Part of paid clinical trials in Wilmington, Delaware.

Sponsor
Chantel Burkitt
Study ID
NCT05764681
Status
Recruiting

Conditions

  • Cerebral Palsy
  • Chronic Post Surgical Pain

Eligibility Criteria

Sex
ALL
Age
5 Years - 17 Years
Healthy Volunteers
Not accepted

Study Details

The study purpose is to document the typical trajectory of perioperative pain experience in Cerebral Palsy (CP) and to identify important predictive factors for the development of chronic postsurgical pain. The main aims of the investigators are to: 1. Quantify the trajectory of pain and opioid use in the context of orthopedic surgery in children with CP. 2. Identify predictors for CPSP in children with CP and develop an applicable risk index. 3. Examine relationships between perioperative pain severity and functional/mobility outcomes achieved by orthopedic surgery in children with CP. Participants will complete: 1. Questionnaires/Surveys via email and text message 2. In-person Sensory Tests 3. In-person Gait and Motion Analysis

Key Dates

Start date
Mar 17, 2023
Status verified
Mar 2025
Primary completion
Feb 29, 2028
Completion
Jan 31, 2029

Study Design

Enrollment
500 participants (estimated)

Primary Outcome Measure

Change in Brief Pain Inventory (BPI) score from 1 week preoperative to 1, 3, 6, and 12 months postoperative [ Time Frame: 1 month preoperative, and 1, 3, 6, and 12 months postoperative ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Nemour's Children's HospitalWilmingtonDelaware19803
Wade Shrader, MD
Wade Shrader, MD (PRINCIPAL_INVESTIGATOR)
Gillette Children's Specialty HealthcareSaint PaulMinnesota55101
Chantel Burkitt, PhD
Chantel Burkitt, PhD (PRINCIPAL_INVESTIGATOR)

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