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Chronic Postsurgical Pain (CPSP)

C

Chantel Burkitt

Status

Enrolling

Conditions

Cerebral Palsy
Chronic Post Surgical Pain

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05764681
STUDY00014668
1R01HD108406-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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

Enrollment

500 estimated patients

Sex

All

Ages

5 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • CP diagnosis
  • Have a scheduled lower extremity or spine orthopedic surgery

Exclusion criteria

  • Non-English speaking and reading parent/guardian

Trial contacts and locations

2

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Central trial contact

Maykala Owens; Lisa Lykken

Data sourced from clinicaltrials.gov

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