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临床试验/NCT07116408
NCT07116408招募中4 期

Intranasal Sphenopalatine Ganglion Blockade as a Non-invasive, Opioid-sparing Treatment for Headaches Following Aneurysmal Subarachnoid Hemorrhage

Wright State University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2024年5月20日最近更新:
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
20
试验地点
2
主要终点
Headache severity

研究概览

简要总结

In patients with bleeding from a brain aneurysm, severe headache is the most common complaint. However, the pain is difficult to treat. The use of standard pain medications is common, but pain control remains poor. Additionally, pain medicines have multiple side effects including sedation, interference with breathing, intestinal cramping, low blood pressure, and the risk of addiction. In the present study, the investigators will examine the use of a medication to block the sphenopalatine ganglion which is a bundle of nerves that includes nerves that cause head pain. This block is performed by spraying numbing medication into the back of the nasal cavity on both sides. This particular pain medication does not have the side effects discussed above. The purpose of the study is to see if this treatment will decrease pain without causing unwanted side effects.

All patients in the study will receive standard pain medicine as needed for headache. Information will be collected from the patient's medical chart on the amount of pain medication used and the amount of pain the patient describes having. The average pain will be calculated for the first 24 hours the patient is in the hospital. At that point, the patient will receive pain medication sprayed into the back of the nasal cavity on both sides. Patients will also receive this treatment 3 days later. Following these treatments, information will be obtained on the average amount of pain, and how much other pain medication is used.

The investigators will look at the amount of pain and the amount of other pain medicine used over the first 24 hours before the nasal pain medicine treatment and compare it to the time after the treatments to see if the amount of pain decreases and if the amount of other pain medicine needed decreases as well. Six months after discharge, the patient will be contacted by phone to find out more information about how much head pain they had after discharge from the hospital.

详细描述

Spontaneous subarachnoid hemorrhage (SAH) accounts for up to 8% of strokes and affects approximately 30,000 individuals yearly in the US alone. Of those, ruptured intracranial aneurysm is the etiology up to 85% of the time. In these patients, severe headache is the most common complaint and its treatment is difficult and often inadequate. However, adequate. Opioids, often in escalating doses, are guideline recommended, but unfortunately they have significant side effects and are often not effective. There have been numerous trials looking at different treatments for the headache caused by SAH. There is an urgent need for an effective treatment with tolerable side effects. The pathophysiology of pain in aneurysmal subarachnoid hemorrhage (aSAH) is not well elucidated.

It is likely related to vasoactive and inflammatory byproducts of blood degradation in the subarachnoid space. The intracranial vessels themselves are abundantly innervated, predominantly by branches of the maxillary nerve. The sphenopalatine ganglion (SPG) is a possible target for intervention, as blockade has been shown to be effective in cluster headaches. The SPG is located near the maxillary nerve, which may explain why blockade is also useful in several other head pain disorders. A small, single center pilot study of seven patients evaluated a bilateral suprazygomatic pterygopalatine fossa blockade as a treatment for headache, and all the patients had clinically significant reductions in reported pain. This study aims to evaluate whether intranasal SPG blockade could provide an effective and minimally invasive treatment option to improve pain and possibly reduce opioid requirements in these patients.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged 18 years or older who are being treated in the neurologic ICU for subarachnoid hemorrhage with Hunt and Hess scale of 0-3 (Scale ranges from 0 to 5 with higher numbers indicating more severe symptoms) and able to verbally report headache will be considered for inclusion in this study.

排除标准

  • Patients under the age of 18 years of age.
  • Patients with an allergy to lidocaine.
  • Patients from all vulnerable groups.
  • Patients with Hunt and Hess scale score of 4-
  • (Scale ranges from 0 to 5 with higher numbers indicating more severe symptoms.)
  • Patients who are not able to consent.
  • Mentally impaired patients that are unable to provide consent.
  • Patients that are prisoners.
  • Pregnant patients.
  • Additionally, patients with contraindications to use of the Tx 360 device will be excluded. Contraindications include:
  • History of recurrent nose bleeds.
  • Nasal septal deformity such as cleft lip and palate, choanal atresia (narrowed nasal passages), atrophic rhinitis, rhinitis medicamentosa, septal perforation, nasal/midface trauma.
  • Recent nasal/sinus surgery
  • Presence of a bleeding disorder (eg., Von Willebrand's disease or hemophilia).
  • Severe respiratory distress.
  • Presence of angiofibroma, sinus tumor, or granulomatous disease of the nasopharynx.
  • Presence of nasal trauma.
  • Nasal congestion that has been present more than 10 days, high fever, or abnormal appearance of the nasal mucosa or mucus.

研究组 & 干预措施

Treatment arm

Experimental

Treatment arm

干预措施: Lidocaine (drug) (Drug)

Treatment arm

Experimental

Treatment arm

干预措施: Tx 360 (Device)

结局指标

主要结局

Headache severity

时间窗: Day 1 (day of consent) Patient receives first treatment. Pain will be recorded every 8 hours. Second treatment is on day 4. Pain will be recorded every 8 hours until discharge from the ICU, an average of 2 weeks, and at 6 months post discharge.

Description of headache severity using the headache numerical rating scale. The scale is a subjective rating of headache pain. The scale ranges from 0-10 with 0 being no pain (minimum value, better outcome) and 10 being the worst pain imaginable (maximum value, worse outcome).

次要结局

  • Opioid dose(2 weeks (or duration of hospitalization))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

John Terry

Associate professor of Neurology

Wright State University

研究点 (2)

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