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NCT07062367

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

Recruiting now NA Last updated 14 July 2025
What this trial tests

NA trial testing Propofol in Sevoflurane in 90 participants. Currently enrolling.

Timeline
1 February 2025
Primary endpoint
1 February 2027
1 February 2027

Quick facts

Lead sponsorTanta University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment90
Start date1 February 2025
Primary completion1 February 2027
Estimated completion1 February 2027
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Tanta University

Who can join

Adults 18 to 65, female only, with Sevoflurane or Lidocaine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Propofol

Trials testing the same drug.

Other recruiting trials for Sevoflurane

Currently open trials in the same condition.

Other Tanta University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07062367.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing