COMPARING THE EFFICACY OF SPHENOPALATINE GANGLION BLOCK FOR TREATMENT OF POSTDURAL PUNCTURE HEADACHE USING 2 percent LIGNOCAINE SPRAY NASALLY AMONG OBSTETRIC POPULATION: RANDOMIZED CONTROLLED TRIAL.
试验速览
- 阶段
- Phase 3 4
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Pain relief, measured using a visual analog scale (VAS) for headache
研究概览
简要总结
The aim of this study is to evaluate the efficacy and efficiency of
sphenopalatine ganglion block (SPGB) in the management of post-dural
puncture headache (PDPH) in obstetric patients.
Primary objective
- Assess the Efficacy of SPGB in Relieving PDPH
Measure the degree of pain relief in obstetric patients following
SPGB administration.
Compare the pain relief outcomes of SPGB with other
conventional treatments for PDPH.
Secondary objective
- Evaluate the Efficiency of SPGB in Terms of Time to Relief
Determine the average time taken for SPGB to provide pain relief
compared to other treatments.
the duration of pain relief provided by SPGB.
- Examine Patient Outcomes and Satisfaction
Assess patient-reported outcomes including pain scores, quality of
life, and overall satisfaction with SPGB treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- Female
入选标准
- •Obstetric patients experiencing PDPH following spinal anesthesia.
- •• Young patients (aged 18-40) experiencing PDPH following lumbar puncture after spinal anesthesia.
- •• Patients who provide informed consent to participate in the study.
排除标准
- •Patients with contraindications to SPGB, such as severe nasal septum deviation or active nasal infection.
- •Patients with a history of allergy to local anesthetics.
- •Patients with significant comorbid conditions that may interfere with study outcomes.
- •• Patients who decline to participate or withdraw consent during the study.
结局指标
主要结局
Pain relief, measured using a visual analog scale (VAS) for headache
时间窗: Pain relief, measured using a visual analog scale (VAS) for headache | intensity at multiple time points: baseline, 30 minutes, 1 hour, 6 hours, | 12 hours, 24 hours, and 48 hours post-intervention.
intensity at multiple time points: baseline, 30 minutes, 1 hour, 6 hours,
时间窗: Pain relief, measured using a visual analog scale (VAS) for headache | intensity at multiple time points: baseline, 30 minutes, 1 hour, 6 hours, | 12 hours, 24 hours, and 48 hours post-intervention.
12 hours, 24 hours, and 48 hours post-intervention.
时间窗: Pain relief, measured using a visual analog scale (VAS) for headache | intensity at multiple time points: baseline, 30 minutes, 1 hour, 6 hours, | 12 hours, 24 hours, and 48 hours post-intervention.
次要结局
- Evaluate the Efficiency of SPGB in Terms of Time to Relief(Determine the average time taken for SPGB to provide pain relief compared to other treatments.)
研究者
Dr Rohit Parashar
Dr. S.N Medical college, Jodhpur