Actively Recruiting

Phase Not Applicable
Age: 20Years - 70Years
All Genders
ID06816641

Surgical Evacuation Of Spontaneous Intracerebral Hematoma: Clinical Outcomes and Prognostic Factors

Led by Sohag University · Updated on 2025-02-11

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates surgical removal of spontaneous intracerebral hemorrhage (ICH), a severe stroke type caused by bleeding into the brain tissue. ICH can cause brain injury from pressure effects and secondary cellular damage, with risks linked to high blood pressure and amyloid buildup in brain vessels. The study aims to assess the safety and effectiveness of surgery to remove the blood clot and prevent further brain injury, especially focusing on early intervention and modern minimally invasive techniques. Participants receive surgical evacuation of the intracerebral hematoma through craniotomy or minimally invasive methods. The surgery is intended to relieve pressure on brain tissue and reduce damage from blood products. Although surgery carries risks such as bleeding and infection, this trial evaluates outcomes after surgical removal of the hematoma, including clinical results and factors affecting prognosis. During the study, participants are monitored for morbidity and mortality at one and three months after surgery. Researchers assess clinical outcomes and complications, tracking recovery progress and survival rates. The total participation spans from surgery through follow-up visits to evaluate short- and medium-term effects of the surgical treatment on brain hemorrhage patients.

CONDITIONS

Brief Title

Surgical Evacuation Of Spontaneous Intracerebral Hematoma: Clinical Outcomes and Prognostic Factors

Who Can Participate

Age: 20Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with radiological findings of spontaneous intracerebral hemorrhage
  • Age between 20 and 70 years
Not Eligible

You will not qualify if you...

  • Traumatic intracerebral hemorrhage, ruptured aneurysm, arteriovenous malformation, or brain tumor
  • Intracerebral hemorrhage after cranial surgery
  • Secondary hydrocephalus
  • Liver cell failure or renal cell failure
  • Bleeding disorders
  • Regular use of anticoagulant or antiplatelet therapy
  • Small intracerebral hemorrhage size less than 30 ml
  • Glasgow Coma Scale less than 6 before surgery

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to several days post-surgery

Participants undergo surgical evacuation of intracerebral hemorrhage followed by immediate post-operative care to manage and monitor recovery.

1 surgery and immediate hospital stay

Post-operative Follow-up

Duration - 3 months

Participants are monitored for morbidity and mortality outcomes after surgical evacuation of intracerebral hematoma.

Follow-up visits at 1 month and 3 months post-surgery

Trial Site Locations

Total: 1 location

1

Sohag University hospitals

Sohag, Egypt

Actively Recruiting

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Research Team

M

Mohamed A Ragheb, Demonstrator

A

Ahmed S Mohamed, Professor

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Published Research Related To This Trial

Incidence, case fatality, and functional outcome of intracerebral haemorrhage over time, according to age, sex, and ethnic origin: a systematic review and meta-analysis.

Charlotte Jj van Asch, Merel Ja Luitse, Gabriël Je Rinkel...

https://pubmed.ncbi.nlm.nih.gov/20056489