Actively Recruiting

Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID06464419

Ultrasonographic Evaluation of Optic Nerve Sheath Diameter in Patients Undergoing Retrograde Intrarenal Surgery in the Lithotomy Position

Led by Başakşehir Çam & Sakura City Hospital · Updated on 2024-08-05

52

Participants Needed

1

Research Sites

3 weeks

Total Duration

On this page

Sponsors

B

Başakşehir Çam & Sakura City Hospital

Lead Sponsor

A

Ankara Etlik City Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to study how the lithotomy position affects intracranial pressure by measuring the optic nerve sheath diameter using ultrasound. The focus is on patients undergoing retrograde intrarenal surgery (RIRS), with attention to the possible increase in venous return and intra-abdominal pressure that this position may cause. The study explores these effects because the lithotomy position may compress venous structures and increase pressure inside the extremities and the head. Participants in this observational study are patients having RIRS surgery performed while in the lithotomy position. The study uses ultrasound to measure the optic nerve sheath diameter during surgery and again ten minutes after the operation to assess changes related to intracranial pressure. No additional treatments or medications are administered as part of this study. Throughout the study, participants will undergo ultrasound evaluations to monitor the optic nerve sheath diameter intraoperatively and postoperatively. Researchers will record these measurements to understand if and how the lithotomy position influences intracranial pressure. The observation period is limited to the time during and shortly after surgery, with overall participation lasting only as long as the surgical and immediate postoperative assessments.

CONDITIONS

Brief Title

Effect of Lithotomy Position on Optic Nerve Sheath Diameter

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Day of surgery and immediate postoperative period

Participants undergo retrograde intrarenal surgery in the lithotomy position, during which the optic nerve sheath diameter is measured by ultrasound intraoperatively and 10 minutes postoperatively to evaluate changes in intracranial pressure.

1 surgery visit and 1 postoperative ultrasound assessment

Trial Site Locations

Total: 1 location

1

EtlikCityHospital

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

C

Cansu Ekici

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Ultrasonographic measured optic nerve sheath diameter as an accurate and quick monitor for changes in intracranial pressure.

Iscander M Maissan, Perjan J A C Dirven, Iain K Haitsma...

https://pubmed.ncbi.nlm.nih.gov/25955869

Changes in intraocular pressure and optic nerve sheath diameter in patients undergoing robotic-assisted laparoscopic prostatectomy in steep 45° Trendelenburg position.

Sebastian Blecha, Marion Harth, Felix Schlachetzki...

https://pubmed.ncbi.nlm.nih.gov/28284189