Does short or long-Term Teriparatide therapy enhance fusion in patients undergoing TLIF? A Randomised controlled trial
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- -Spinal fusion rate at 1 year, assessed by computed tomography (CT) scan using the Brantigan-Steffee-Fraser (BSF) criteria and Bridwell criteria for fusion.
研究概览
简要总结
**Background:**Lumbar degenerative diseases often require Transforaminal Lumbar Interbody Fusion (TLIF), but complications such as non-union (pseudarthrosis) can occur, particularly in osteoporotic patients.Teriparatide, a recombinant human PTH analog, is hypothesized to improve spinal fusion by stimulating bone formation, making it a potential therapeutic agent for reducing complications.**Study Objectives:**Primary Objective: Compare spinal fusion rates at 6 months and 1 year postoperatively between a Teriparatide-treated group and a control group.Secondary Objectives: Assess clinical outcomes (e.g., disability and pain scores), bone mineral density changes (via DEXA scans), mechanical complications, and any adverse events.**Study Design:**Type: Randomized controlled trial (RCT)Duration: 24 months (12-month follow-up post-surgery)Population: 100 patients undergoing TLIF for lumbar degenerative conditions, randomized equally into a study (teriparatide) group and a control group.**Methodology:**Intervention: The study group receives daily teriparatide (20 mcg subcutaneously) along with calcium and vitamin D3 supplementation. The control group receives only calcium and vitamin D3.Monitoring Tools: CT scans, DEXA scans, and clinical questionnaires (ODI, VAS, SF-36, Roland-Morris Disability Questionnaire).**Outcome Measures:**Primary Endpoint: Spinal fusion rate, evaluated by CT scans using standard criteria.Secondary Endpoints: Improvement in pain and functional scores, bone mineral density changes, and complication rates (e.g., screw loosening, cage subsidence).**Inclusion and Exclusion Criteria:**Inclusion: Patients aged ≥45 years undergoing single-level TLIF for degenerative spine diseases.Exclusion: Prior lumbar surgeries, teriparatide use, and contraindications (e.g., hypercalcemia, Paget’s disease).**Data Analysis:**Primary Analysis: Fusion rate comparisons.Secondary Analysis: Assessment of disability scores, complications, and adverse events using statistical models.**Expected Outcomes:**The study aims to demonstrate that teriparatide therapy significantly enhances spinal fusion rates and clinical outcomes while maintaining a favorable safety profile, potentially establishing it as a preferred treatment adjunct in TLIF surgeries.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 45.00 Year(s) 至 75.00 Year(s)(—)
- 性别
- All
入选标准
- •Age 45 years or older -Undergoing elective single level TLIF for degenerative spine diseases -No contraindications for teriparatide.
排除标准
- •Preoperative use of teriparatide -Contraindications to use of teriparatide (e.g., hypercalcemia, bone metastasis, Paget disease) -History of prior lumbar surgery at the index level -Infections, tumors, trauma.
结局指标
主要结局
-Spinal fusion rate at 1 year, assessed by computed tomography (CT) scan using the Brantigan-Steffee-Fraser (BSF) criteria and Bridwell criteria for fusion.
时间窗: one year
次要结局
- Clinical outcomes: ODI and VAS scores, SF-36 (for overall health-related quality of life), or the Roland-Morris Disability Questionnaire for lumbar spine patients, to capture more comprehensive patient-reported outcomes at 3, 6, and 12 months post surgery(-Monitor DEXA scan: results for changes in bone mineral density (BMD) across groups to evaluate the effectiveness of calcium and vitamin D3 in comparison to teriparatide and combination therapy.)
研究者
Dr Sudhir G
Sri Ramachandra Institute of Higher Education and Research
