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Incidence of Intraoperative brain swelling in adult patients undergoing elective brain surgeries

Incidence and Risk Factors of Intraoperative Brain Swelling in adult patients undergoing elective craniotomies- A Prospective Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/05/053017
Enrollment
400
Registered
2023-05-22
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: G978- Other intraoperative and postprocedural complications and disorders of nervous system

Interventions

Control Intervention1: Nil: NIL

Sponsors

NIMHANS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients age >18 y undergoing craniotomy for lective neurosurgical procedures

Exclusion criteria

Exclusion criteria: Patients undergoing Redo/Reexploration Surgeries (within 2 weeks of the first surgery) Patients undergoing Stereotactic Biopsy/ Emergency Surgery Patients undergoing Deep Brain Stimulation and Ablation procedures Patients undergoing Endoscopic procedures. Patients undergoing burr hole evacuation of blood clots and ventriculoperitoneal shunt procedures.

Design outcomes

Primary

MeasureTime frame
To determine the incidence of intraoperative brain swelling in adult patients undergoing elective craniotomy.Timepoint: at opening of duramater, during surgery, at closure 1: Brain below the duramater 2: Brain at the level of the duramater 3: Brain above the level of the duramater, pulsating. Surgeon proceeds with the surgery not asking for any intervention. 4: Brain above the level of the dura and firm. Surgeon hesitant to proceed with the surgery without any intervention.

Secondary

MeasureTime frame
1. To study the risk factors for development of intraoperative brain swelling. 2. To compare the postoperative neurological complications in patients with and without intraoperative brain bulge. 3. To compareâ??the effect of intraoperative brain bulge on the patientsâ?? outcome at hospital discharge.Timepoint: Outcome at the time ofICU discharge (GOS-E): Outcome at the time of hospital discharge (GOS-E):

Countries

India

Contacts

Public ContactShiva Keshava Murthy A

Department of Neuroanesthesia and Neurocritical care, NIMHANS

mrks1974@gmail.com

Outcome results

None listed

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