Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07307508

Efficacy of Scalp Block in Managing Post Subarachnoid Hemorrhage Headache in Critically Ill Patients. A Single Centre Randomized Controlled Trial

Led by Hamad Medical Corporation · Updated on 2025-12-29

22

Participants Needed

1

Research Sites

62 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Subarachnoid hemorrhage (SAH) is a devastating neurological disorder associated with significant mortality and morbidity rates, arising not just from the hemorrhage itself but also because of the catastrophic multisystem sequelae that can accompany the condition. Rupture of an intracranial aneurysm accounts for up to 85% of instances of SAH, occurring in approximately 3 to 25 people per 100,000 annually in most populations. Treatment of aneurysmal SAH (aSAH) includes prevention of re-bleeding, evacuation of space-occupying hematomas, management of hydrocephalus, and prevention of secondary cerebral insult. Severe headache is the predominant characteristic symptom of aSAH, developing almost instantaneously at ictus in 50% of cases and continuing into the first days. Its severity has a variety of physiological and psychological effects on the patient. Scalp blocks have been suggested to alleviate this headache in case series. However, there is no strong evidence supporting this intervention. In this study, we aim to assess the impact of scalp blocks on headache reduction in patients undergoing endovascular treatment of an aneurysm (coiling or flow diversion) with aneurysmal subarachnoid bleeding.

CONDITIONS

Official Title

Efficacy of Scalp Block in Managing Post Subarachnoid Hemorrhage Headache in Critically Ill Patients. A Single Centre Randomized Controlled Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over 18 years old admitted to the Surgical Intensive Care Unit with confirmed aneurysmal subarachnoid hemorrhage
  • Undergoing endovascular treatment of the aneurysm (coiling or flow diversion)
Not Eligible

You will not qualify if you...

  • Patients undergoing surgical craniotomy and aneurysmal clipping
  • Non-aneurysmal or other types of intracranial hemorrhage
  • Glasgow Coma Scale score of 13 or lower upon SICU admission
  • WFNS score 4 or 5 or requiring mechanical ventilation for more than 24 hours
  • Known allergy to local anesthetics
  • Admission to ICU more than 7 days after hemorrhage
  • Documented bleeding disorders
  • History of chronic headache disorder or migraine
  • Pregnancy

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hamad Medical Corporation

Doha, Qatar

Actively Recruiting

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Research Team

S

Sohel Mohamed Ahmed, Consultant

CONTACT

A

Abdelrahman Balal, Clinical Fellow

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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