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Effect of Lithotomy Position on Optic Nerve Sheath Diameter

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Başakşehir Çam & Sakura City Hospital

Status

Enrolling

Conditions

Intracranial Pressure Increase
Optic Nerve Cup

Treatments

Device: ultrasound

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

In this study, the effect of increased venous return and increased intra-abdominal pressure on intracranial pressure in the lithotomy position was evaluated.

Full description

In the lithotomy position, it is possible that venous return in the lower extremities increases and intra-abdominal pressure increases due to the position. At the same time, it is possible that the intracompartmental pressure in the extremities increases because the venous structure is compressed by placing the lower extremities on supports. Considering both conditions, it is predicted that there may be an increase in the optic nerve sheath diameter due to increased intracranial pressure in patients placed in the lithotomy position. The aim of this study is to investigate the effect of the position on intracranial pressure by ultrasonographically evaluating the optic nerve sheath diameter in the lithotomy position.

Enrollment

52 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who give informed consent
  • Patients who will undergo retrograde intrarenal surgery
  • Patients who are fully oriented and cooperative
  • ASA I-II patients
  • Patients between the ages of 18-65

Exclusion criteria

  • Disoriented and uncooperative patients
  • Patients with BMI>30
  • Patients who have had previous intracranial surgery
  • Patients who have had eye surgery before
  • Patients allergic to the pharmacological agents used in the study

Trial design

52 participants in 1 patient group

Patients who will undergo RIRS surgery
Description:
Patients who will undergo RIRS surgery in the lithotomy position
Treatment:
Device: ultrasound

Trial contacts and locations

1

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Central trial contact

Cansu Ekici

Data sourced from clinicaltrials.gov

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