Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06819657

Safety , Feasibility and Preliminary Efficacy of Remote Ischemic Conditioning in Patients With Aneurysmal Subarachnoid Hemorrhage After Aneurysm Clipping

Led by Beijing Tiantan Hospital · Updated on 2025-09-09

40

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study was designed to evaluate the safety and efficacy of remote ischemic conditioning (RIC) in patients with aneurysmal subarachnoid hemorrhage (aSAH) following surgical clipping. Aneurysmal subarachnoid hemorrhage is a life-threatening condition that occurs when a cerebral aneurysm ruptures, causing bleeding into the subarachnoid space. Surgical clipping of the aneurysm is a standard procedure used to stop the bleeding and prevent re-rupture, thereby stabilizing the patient's condition. Remote ischemic conditioning (RIC) is a non-invasive treatment that involves using a blood pressure cuff to induce brief, temporary cycles of ischemia and reperfusion in a limb. Research suggests that this process may confer systemic protective effects, potentially improving recovery from brain injury or surgery. Although RIC has shown potential to improve outcomes in patients with other neurological conditions, its effect on patients with aSAH who undergo surgical clipping remains unclear. This study will evaluate whether RIC can reduce complications, improve neurological function, and enhance overall recovery in these patients. The findings will help determine whether RIC should be incorporated into the standard treatment regimen for aSAH.

CONDITIONS

Official Title

Safety , Feasibility and Preliminary Efficacy of Remote Ischemic Conditioning in Patients With Aneurysmal Subarachnoid Hemorrhage After Aneurysm Clipping

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Imaging confirmed aneurysmal subarachnoid hemorrhage
  • Aneurysm treated with craniotomy clipping within 24 hours
  • Age between 18 and 80 years old
  • Informed consent given by participant or legal representative
Not Eligible

You will not qualify if you...

  • Other types of cerebral hemorrhage
  • Prior neurological impairment with mRS score greater than 1 or mental illness interfering with assessments
  • Severe comorbid conditions with life expectancy under 90 days
  • Refractory hypertension with systolic >180 mmHg or diastolic >110 mmHg
  • Severe soft tissue injury of lower limbs contraindicating RIC
  • Participation in another experimental therapy study
  • Any condition increasing patient risk as judged by the investigator

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Trial Site Locations

Total: 1 location

1

Beijing Tiantan Hospital

Beijing, Beijing Municipality, China, 100000

Actively Recruiting

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Research Team

A

Aihua Liu, Doctor

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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