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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04833530
Other study ID # 0010-21
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 1, 2021
Est. completion date December 1, 2022

Study information

Verified date March 2021
Source Rabin Medical Center
Contact Sharon Orbach-Zinger
Phone 972 54-538-3093
Email sharonorbach@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pulmonary aspiration is one of the most serious risks of general anesthesia and has been reported to occur in as many as 1 in 4000 cases of general anesthesia. Gastric ultrasound is an emerging point-of-care tool that provides bedside information on gastric content and volume. There have been a few factors which are thought to increase gastric size. Delayed gastric emptying such as caused by gastroparesis in Diabetes Mellitus is an example. Certain surgeries also cause gastroparesis. Other preoperative factors including pain, preoperative anxiety, and blood levels of estradiol or progesterone are less well studied.


Description:

Women will be recruited before undergoing the procedure. Upon signed informed consent, women will be asked to rank their anxiety level on a scale of 0-10 (Verbal Numeric Anxiety Score). This scale has been used for previous studies to assess anxiety (Orbach-Zinger, Danon) In the operating room, a gastric ultrasound will be performed in the supine position and the antral cross sectional area will be measured. This study is purely observational, the gastric ultrasound assessment is non-invasive and will not cause any adverse effects or discomfort to the patient. Participation in the study will not affect clinical management in any way. Each one of the ultrasound assessments will be performed by one of the study's' investigators. Anesthesia will be induced in standard procedure and positive pressure will be instituted according to the standard protocol accepted in our hospital. At the end of the procedure, the gastric ultrasound circumference will be measured again.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date December 1, 2022
Est. primary completion date April 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 120 Years
Eligibility Inclusion Criteria: Woman aged 18 and above undergoing general anesthesia for oocyte retrieval during in vitro fertilization with the ability to sign an informed consent. Exclusion Criteria: 1. Women with BMI >40 2. Women with diabetes 3. Women who have previously undergone gastric surgery 4. Women with language barriers.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Gastric Ultrasound
In the operating room, a gastric ultrasound will be performed in the supine position and the antral cross sectional area will be measured. Anesthesia will be induced in standard procedure and positive pressure will be instituted according to the standard protocol accepted in our hospital. At the end of the procedure, the gastric ultrasound circumference will be measured again.

Locations

Country Name City State
Israel Beilinson hospital Petach tikvah

Sponsors (1)

Lead Sponsor Collaborator
Rabin Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Preoperative gastric ultrasound measurement Within 24 hours before Oocyte pickup
Primary Post-anesthesia gastric ultrasound measurement During Oocyte pickup 1 hour
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