Sevoflurane With or Without Intravenous Lidocaine Infusion Versus Propofol Anesthesia on Intracranial Pressure and Cerebral Oxygenation During Laparoscopic Hysterectomy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-65
SponsorTanta University

About this trial

This study will be conducted to evaluate the effects of different anesthetic modalities \[sevoflurane with or without intraoperative lidocaine infusion and Propofol total intravenous anesthesia (TIVA)\] on intracranial pressure (ICP) and cerebral oxygenation assessed by non-invasive methods during laparoscopic hysterectomy (LH).

Eligibility criteria

Qualifiers

Age from 18 to 65 years.

American Society of Anesthesiologists (ASA) physical status I and Ⅱ.

Body mass index (BMI) ≤35.

Females scheduled for laparoscopic hysterectomy.

Disqualifiers

Patients' refusal to participate in the study.

Hypersensitivity and allergy to drugs of the study.

Contraindication for optic nerve sheath diameter assessment. E.g., patient with pre-existing ophthalmic diseases, a history of ophthalmic surgery

Any central nervous system or cardiovascular disease, severe hepatic or renal impairment

Trial design

Treatments tested in this trial

  • Propofol
  • Sevoflurane plus lidocaine infusion
  • Sevoflurane

Treatment groups

90 Participants
are divided into 3 treatment groups

Sponsors and collaborators