Comparative study of trigger point injection versus stellate ganglion block in chronic shoulder-facial myofascial pain syndrome
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 52
- 试验地点
- 1
- 主要终点
- visual analogue scale
研究概览
简要总结
After the study was approved by the ethical committee members, the patients were
informed about the study procedure and written informed consent was
obtained.Patients suspected to have craniofascial myofascial pain of all degrees of
severity were included. Patients diagnosed by clinical and imaging modalities in pain
OPD of institute of medical sciences -banaras hindu university.The patient’s vital
signs should be monitored before and immediately following the procedure.
A peripheral venous catheter should be placed in all patients. It is important to obtain
a detailed medical history before the procedure to rule out any contraindications and
evaluate the risk/benefits ratio.
1.USG GUIDED TRIGGER POINT INJECTION
After standard aseptic precautions high frequency linear usg probe would be placed
in the logitudinal and transverse plane to look for any changes in the muscle
underlying the spot marked on the skin. After anaesthetizing the skin with 1%
lidocaine, 22g 50mm stimuplex needle would be inserted in to the triggerpoint.
Trigger points are hypoechoic in nature.if the needling of suspected visible area
reproduced the pain normally experienced by the patient it is called needle sign.
Before injecting drug aspiration would be done to ensure that needle is not in the
vascular structure. Then 2-3 ml of bupivacaine 0.25% with dexamethazone 0.1mg/kg
would be injected into the trigger point.
2.USG GUIDED STELLATE GANGLION BLOCK
The patient would be supine with the neck slightly extended and the head slightly
rotated contralaterally to the approached side. After standared aseptic precaution
transducer would be placed perpendicular to the tracheal axis at the cricoid cartilage
slinding inferiorly until the superior aspect of the thyroid gland is visualized and
relocated laterally to the anterior aspect of the Chassaignac’s tubercle on the C6
transverse process. Color Doppler would be used to detect the position of the vessels.
With an in-plane approach, the needle would be placed adjacent to trachea , The tip of
the neede would be in prevertebral fascia of the Longus colli muscle . Proper
positioning of needle would be confirmed by hydrodissection,5ml of a local
anesthetic 0.25 % bupivacaine+ dexamethazone would be injected along the
paravertebral fascia to the stellate ganglion.The block would also be clinically
confirmed by ipsilateral Horner’s syndrome (ptosis, miosis, and anhydrosis), flushing
of the face, and increased temperature of the arm.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 65.00 Year(s)(—)
- 性别
- All
入选标准
- •1.patients with symptoms for more than 3 months 2.ASA grade 1 and 2.
排除标准
- •1.patients with symptoms less than 3 months 2.ASA grade 3 and more 3.patients with known allergy to local anaesthetics.
结局指标
主要结局
visual analogue scale
时间窗: post procedure outcomes are assessed immediate, 1week, 1month, 3months
次要结局
- General health questionnaire-(GHQ-12)
研究者
Dr J Manikandan
Institute Of Medical Sciences, Banaras Hindu University
