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Intracranial pressure changes with dexmedetomidine in patients undergoing laparoscopic hysterectomy

Intracranial pressure changes with dexmedetomidine in patients undergoing laparoscopic hysterectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202601484722115
Enrollment
50
Registered
2026-01-30
Start date
2024-06-16
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Anaesthesia

Interventions

normal saline as placebo
dexmedetomidine

Sponsors

anesthesia intensive care and pain management department. faculty of medicine menoufia university egypt
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: • Patients who are scheduled for laparoscopic hysterectomy. • Age from 35 to 65 years old. • American Society of Anesthesiologists (ASA ) I-II. • Body mass index (BMI) from 18.5 to 25 kg/m2.

Exclusion criteria

Exclusion criteria: • Patient refusal to participate. • Inappropriate temporal window for transcranial Doppler (TCD) measurement, cerebrovascular disease and/or increased intracranial pressure. • Respiratory diseases (Restrictive or Obstructive). • Uncontrolled hypertension ( > 140/90) or vascular diseases. • Heart block, bradyarrthymia. • Patients on ß blockers. • Procedures lasting less than 90 minutes. • Patients whose CO2 pneumoperitoneum and trendelenburg position are interrupted or converted to open technique. • Patients who have a history of allergy to a2 agonists or to any of the study drugs. • Patients who have eye diseases. • Patients whose ultrasound scans or measurements fail to clearly show the structure of ONSD.

Design outcomes

Primary

MeasureTime frame
intracranial pressure ICP) measured using optic nerve sheath diameter (ONSD).

Secondary

MeasureTime frame
pulsatility index from transcranial doppler;• Mean arterial pressure (MAP). • Heart rate. ;• Duration of pneumoperitonium. • Duration of trendelenburg position. • Intraoperative blood loss. • The volume of administered fluids. • EtCO2. • Extubation time (minutes from switch off isoflurane until the patient fulfills the global and respiratory criteria for safe extubation as breathing with a minimum tidal volume of 7 ml/kg, ability to sustain 5 seconds head lift, sustained hand grip, sustained arm lift). • PACU discharge time in minutes.

Countries

Egypt

Contacts

Public Contactkhaled gaballah

assistant professor

khgaballah@gmail.com01016009073

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026