- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06048900
Evaluation of the Effect of Trendelenburg Position Duration on Intracranial Pressure
September 19, 2023 updated by: Dilek Cetinkaya
Evaluation of the Effect of Trendelenburg Position Time on Intracranial Pressure in Laparoscopic With Ultrasonographic Optic Nerve Sheath Diameter Measurement
The Lloyd Davies position is a position used in laparoscopic hysterectomies where the head is lowered 45 degrees and the legs are bent from the knee area.It is a version of the Trendelenburg position.
Both this position and for laparoscopic surgery carbon dioxide (CO2) gas given into the abdomen, causes problems for the patient.
Increased abdominal and thoracic pressure impairs venous return and increases intracranial pressure.
Optic nerve sheath diameter can be measured by placing an ultrasound probe over the eye.
It is possible to follow up the increase in intracranial pressure with this diameter measurement.
In this study, it was planned to measure the optic nerve sheath diameter by ultrasound in patients who will undergo laparoscopic hysterectomy.
It is aimed to observe the changes in the increase in intracranial pressure as the time lengthens with the measurements to be made at certain intervals during the operation.
Secondary aim is to determine whether there is a cut-off value where the intracranial pressure starts to increase.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The Trendelenburg position is the patient's head down with the table tilted, with the head closer to the floor than the feet.
Lloyd Davies position is a modified version of the Trendelenburg position, used especially in laparoscopic hysterectomies, where the head is lowered 30-45° and the legs are bent at knee level.
During this surgery, pneumoperitoneum is also applied by administering carbon dioxide (CO2) into the abdomen.
During this surgery, pneumoperitoneum is also applied by administering CO2 into the abdomen.
The applied position and intra-abdominal CO2 cause some physiological changes.
These changes include respiratory and cardiac changes as well as increased intracranial pressure.
Optic nerve sheath diameter can be measured by placing an ultrasound probe over the eye.
Increase in intracranial pressure can be followed by sequential measurements.
In this study, it was planned to measure the optic nerve sheath diameter by ultrasound in patients who will undergo laparoscopic hysterectomy.
It is aimed to observe the changes in the increase in intracranial pressure as the time lengthens with the measurements to be made at certain intervals during the operation.
Before the patients were given anesthesia induction, optic nerve sheath diameter measurement (ONSD) was performed by imaging in the sagittal and transverse planes in both eyes in neutral position.
The second measurement was taken 2 minutes after endotracheal intubation in the neutral position.
After the trocars were placed and pneumoperitoneum was applied, the patient was placed in the Lloyd Davies position.
After the position was given, bilateral ONSD measurements were taken at the 30th minute, 60th minute, 75th minute, and 90th minute.
At the end of the surgery, pneumoperitoneum and position were neutralized.
The last measurement was taken 5 minutes after the patient was placed in the neutral position.
Near infrared spectrometry (NIRS) monitoring was performed throughout the surgery.
Study Type
Interventional
Enrollment (Actual)
25
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Odunpazarı
-
Eskisehir, Odunpazarı, Turkey, 26040
- Eskisehir Osmangazi University Medical Faculty
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Patients who will undergo laparoscopic hysterectomy
Exclusion Criteria:
- chronic lung disease, pulmonary hypertension
- glaucoma
- history of eye surgery
- diabetic retinopathy
- intracranial mass,
- hydrocephalus
- history of intracranial surgery
- American society of anesthesiology (ASA) physical classification IV
- optic neuritis
- who do not want to participate in the study.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Optic nerve sheath diameter measurements
A total of 7 measurements were planned to be made at specified times.
|
First, both eyes were measured in a neutral position while awake and after intubation.
Measurements were made at regular intervals until the end of the operation after the head-down position and in the neutral position after the operation.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
optic nerve sheath diameter measurement
Time Frame: during the surgery
|
increase in optic nerve sheath diameter
|
during the surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Timing of increased intracranial pressure
Time Frame: during the surgery
|
If the sheath diameter is over 5 mm, increased pressure will be accepted.
|
during the surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Dilek Çetinkaya, Eskisehir Osmangazi University Medical Faculty
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Chin JH, Seo H, Lee EH, Lee J, Hong JH, Hwang JH, Kim YK. Sonographic optic nerve sheath diameter as a surrogate measure for intracranial pressure in anesthetized patients in the Trendelenburg position. BMC Anesthesiol. 2015 Mar 31;15:43. doi: 10.1186/s12871-015-0025-9. eCollection 2015.
- Ohle R, McIsaac SM, Woo MY, Perry JJ. Sonography of the Optic Nerve Sheath Diameter for Detection of Raised Intracranial Pressure Compared to Computed Tomography: A Systematic Review and Meta-analysis. J Ultrasound Med. 2015 Jul;34(7):1285-94. doi: 10.7863/ultra.34.7.1285.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 10, 2021
Primary Completion (Actual)
September 15, 2022
Study Completion (Actual)
October 15, 2022
Study Registration Dates
First Submitted
September 12, 2023
First Submitted That Met QC Criteria
September 19, 2023
First Posted (Actual)
September 21, 2023
Study Record Updates
Last Update Posted (Actual)
September 21, 2023
Last Update Submitted That Met QC Criteria
September 19, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ESOGU1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
There is not a plan to make individual participant data (IPD) available.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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