Sickle Cell Disease (SCD) Bone Pain Study
NCT05283148 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53
Last updated 2025-08-24
Summary
A prospective study to determine how low bone mineral density and/or vertebral compression fractures associate with pain in adults with sickle cell disease
Conditions
- Sickle Cell Disease
- Sickle Cell Anemia
- Low Bone Density
- Osteoporosis
- Osteopenia
- Vertebral Fracture
- Vertebral Compression
- Osteonecrosis
- Ischemic Necrosis
- Avascular Necrosis
Interventions
- OTHER
-
Dual-energy X-ray absorptiometry
Measure bone mineral density at the lumbar spine, left total hip, left forearm, and whole body
- OTHER
-
Vertebral fracture analysis
Obtain thoracolumbar morphometry in DXA scan, then determine presence and severity of vertebral compression fractures by VFA
- OTHER
-
Adult Sickle Cell Quality of Life Measurement System pain impact questionnaire
Calculate patient-reported total pain scores to determine the pain phenotype of each study participant
Sponsors & Collaborators
-
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH -
Doris Duke Charitable Foundation
collaborator OTHER -
University of California, Davis
lead OTHER
Principal Investigators
-
Oyebimpe O Adesina, MD, MS · UC Davis School of Medicine
Study Design
- Allocation
- NA
- Purpose
- SCREENING
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-03
- Primary Completion
- 2024-04-30
- Completion
- 2026-07-31
Countries
- United States
Study Locations
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