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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04407715
Other study ID # 2018/11-0
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 30, 2019
Est. completion date December 30, 2019

Study information

Verified date May 2020
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Different amounts of anesthetic gas can be used in the obstetric gynecological surgery operations to be performed with open method. Researchers aimed to compare the effect of gas changes on intraocular nerve diameter by ultrasonography.


Description:

A total of 80 patients who underwent laparotomic gynecological surgery were divided into two groups prospectively: high flow of 2 L/min and minimal flow of 0.5 L/min. Anesthesia was maintained with 50% oxygen-50% air at 2 L/min and desflurane at 1.1 MAC in Group 1 (n=40) and with 50% oxygen-50% air at 2 L/min and desflurane at 1.1 MAC in Group 2 (n=40). After 10-15 minutes, group 2 was administered minimal flow with 50-60% oxygen-40-50% air at 0.5 L/min and desflurane, and 10 minutes before the end of the surgery, the patients were switched to high flow with 50% oxygen-50% air at 2 L/min.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date December 30, 2019
Est. primary completion date October 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Aged 18-65 years

- ASA I-II

- Who underwent laparotomic gynecological surgery

Exclusion Criteria:

- Patients with obstructive pulmonary disease

- Patients with decompensated diabetes, those with a fasting period of more than 12 hours -Acute alcohol intoxication

- Chronic alcohol use

- Who refuse to participate in the study

- Who are not cooperative, do not speak Turkish

- Who had known eye disease (glaucoma, retinal detachment), had a previous history of eye surgery,

- Increased intracranial pressure findings (intracranial lesion, previous cerebrovascular diseases

- Body mass index of > 40kg/m2

- ASA > III

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
The Effect Of Minimal and High Flow Anesthesia on Optic Nerve Sheath Diamater
The patients were randomly allocated to one of the two groups of fresh gas flows using the closed-envelope technique: 2 L/min high flow and 0.5 L/min minimal flow.

Locations

Country Name City State
Turkey University of Health Sciences Bursa Yüksek Ihtisas Training and Research Hospital Bursa

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Optic Nerve Sheath Diamater Optic nerve sheath diamater measurements of the patients were recorded before and during the surgery at specified time points (T0: awake, T1: High fresh gas flow after induction at the 10th min., T2: Inhalation anesthesia at the 30th min., T3: Inhalation anesthesia at the 60th min., T4: Inhalation anesthesia at the 90th min., T5: Before extubation).A typical optic nerve sheath is generally less than 5 mm in diameter, and diameters greater than 5.5 mm predict an ICP of =20 cm H2O with 100% sensitivity and specifity 2 hours operation time
Secondary Peroperative Complications Complications during the surgery (decreased oxygen levels, hypercapnia, hypotension, hypertension, bradycardia, tachycardia, rhythm disorders) were recorded. 2 hours operation time
Secondary Postoperative Complications Complications in the recovery room (respiratory distress, decreased oxygen levels, hypotension, hypertension, bradycardia, tachycardia, vomiting, rhythm disorders) were recorded. postop 20 minutes
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