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Denosumab and Screw Fixation for Osteoporotic Compression Fracture

Phase 2
Withdrawn
Conditions
Denosumab Allergy
Interventions
Registration Number
NCT05065164
Lead Sponsor
Shenzhen People's Hospital
Brief Summary

Evaluation of bone mineral density and function at 1 year after screw internal fixation of osteoporotic vertebral compression fractures with desuzumab: a parallel double-blind randomized controlled clinical trial

Detailed Description

Conduct a single-center, double-blind, randomized controlled clinical trial according to clinical Trial Reporting Standards (CONSORT). Bone mineral density and function were compared 1 year after screw internal fixation of osteoporotic vertebral compression fracture (OVCF) with desomumab versus placebo in Shenzhen People's Hospital from September, 2021 to September, 2022. The study was approved by Shenzhen People's Hospital and informed consent was signed

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

• Must be age between 40 and 90 years old

  • X-ray diagnosis of 1-2 vertebral compression fractures
  • Dual energy X ray test bone mineral density T value less than -1
  • fracture history lasted within 6 weeks
  • MRI showed bone marrow edema of injured segment
  • lower back pain, local spines tenderness
Exclusion Criteria
  • • Must be able to have no posterior vertebral wall fracture

    • Must be able to have no patients with intervertebral fissure
    • Must be able to have no infection
    • Must be able to have no malignancy
    • Must be able to have no neurological dysfunction
    • Must be able to have no previous use of anti-osteoporosis drugs within 6 weeks
    • Must be able to have no inability to perform magnetic resonance imaging
    • Must be able to have no prior back surgery
    • Must be able to have no other established contraindications for elective surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
placebo controlDenosumab Only ProductPlacebo subcutaneous injection /6 months, twice a year
dnosumabDenosumab Only ProductDesuzumab 60 mg subcutaneously /6 months, twice a year
Primary Outcome Measures
NameTimeMethod
albuminup to 12 months

serum albumin level

heightup to 12 months

participants height cm

weightup to 12 months

participants weight kg

BMIup to 12 months

participants body mass index

osteocalcinup to 12 months

osteocalcin in the N terminal molecular fragment

Procollagen type 1 n-terminal propeptide P1NPup to 12 months

Procollagen type 1 n-terminal propeptide

C-terminal cross-linked type 1 collagen terminal peptide CTXup to 12 months

C-terminal cross-linked type 1 collagen terminal peptide

Serum total calciumup to 12 months

Serum total calcium level

parathyroid hormoneup to 12 months

serum parathyroid hormone level

sexup to 12 months

participants sex

ageup to 12 months

participants age (year)

lumber spine bone mineral densityup to 12 months

Dual energy X-ray for lumber spine bone mineral density

Hip bone mineral densityup to 12 months

Dual energy X-ray for hip bone mineral density

MRI of lumberup to 12 months

Bone marrow edema and adjacent intervertebral disc were detected by MRI

pain visual analogue scores (VAS)up to 12 months

pain visual analogue scores (VAS) use categories to differentiate pain intensity, with 0 being "painless" and 100 being "the worst pain imaginable".

Secondary Outcome Measures
NameTimeMethod
The Roland-Morris Disability Questionnaireup to 12 month

The Roland-Morris Disability Questionnaire is a health status measure designed to be completed by patients to assess physical disability due to low back pain.

QUALEFFO 31up to 12 month

Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO) was developed in 1997 to evaluate quality of life for patients with osteoporosis

EuroQol-5D (EQ-5D): an instrument for measuring quality of lifeup to 12 month

EQ-5D descriptive system is a preference-based HRQL measure with one question for each of the five dimensions that include mobility, self-care, usual activities, pain/discomfort, and anxiety/depression.

Trial Locations

Locations (1)

ShenzhenPH

🇨🇳

Shenzhen, Guangdong, China

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