Sickle Cell Disease (SCD) Bone Pain Study

NCT05283148 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2025-08-24

Study results available
· View outcomes & findings →

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

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05283148 on ClinicalTrials.gov