ICP Monitoring

Evaluation of effect of intracranial pressure monitoring catheter employment on prognosis of severe head trauma patient in Al Zahra hospital

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180813040788N1

Enrollment

Registered

2019-08-29

Start date

2018-10-23

Completion date

Unknown

Last updated

2019-10-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Intracranial injury. Condition 2: Intracranial injury. Condition 3: Intracranial injury. Condition 4: Intracranial injury. Condition 5: Intracranial injury. Condition 6: Intracranial injury. Condition 7: Intracranial injury. Condition 8: Intracranial injury. Condition 9: Intracranial injury. Concussion Traumatic cerebral edema Diffuse traumatic brain injury Focal traumatic brain injury Epidural hemorrhage Traumatic subdural hemorrhage Traumatic subarachnoid hemorrhage Other

Interventions

Intervention 1: Intervention group: Patients in this group will receive intracranial pressure monitoring catheter (Spiegelberg probe 3PN) and intracranial pressure lowering treatments will be performe

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with consciousness levels of 3 to 8 (based on GCS criteria) and abnormal brain CT scans (including bleeding, cantogens, edema, brain hernia symptoms, or compression of brain cytars) that can be rescued, and patients with a level of consciousness 3 to 8 (based on GCS criteria) and normal brain CT scan older than 40 years of age, systolic blood pressure less than 90 mm Hg, or abnormal motor status in a clinical examination.

Exclusion criteria

Exclusion criteria: Patients who are reluctant to continue studying are excluded.

Design outcomes

Primary

Measure	Time frame
Prognosis of patients with severe brain trauma. Timepoint: Determination of prognosis of patients with severe traumatic brain injury on discharge. Method of measurement: The Glasgow Outcome Scale Extended (GOS-E).	—

Secondary

Measure	Time frame
Surgical site infection. Timepoint: During the hospitalization. Method of measurement: Clinical signs and symptoms and Cultivation of the wound site.;Meningitis. Timepoint: During the hospitalization. Method of measurement: Clinical signs and symptoms and cerebrospinal fluid culture.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaeed Sattaei Mokhtari

Esfahan University of Medical Sciences

saeedmokhtari367@gmail.com+98 31 3620 2020

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026