Ultrasonographic Measurement of Internal Jugular Vein as a Predictor of Hypotension Following Spinal Anesthesia

Spinal Anesthetics Causing Adverse Effects in Therapeutic Use Clinical Trial

— IJV  

Official title:

Department of Anesthesiology and Reanimation, Faculty of Medicine, Osmangazi University, Eskişehir, Turkey

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04486612
• Other study ID #: 10.12.19/43
• Status: Completed
• Start date: January 1, 2020
• Est. completion date: September 24, 2020

Study information

• Verified date: February 2021
• Source: Eskisehir Osmangazi University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Hypotension after spinal anesthesia is associated with significant perioperative morbidity and mortality, especially in hypovolemic patients. Ultrasonographic measurement of internal jugular vein (IJV) has been recently shown as effective in predicting the intravascular volume status. The aim was to investigate the reliability of preanesthetic ultrasound measurements of IJV in predicting hypotension after spinal anesthesia.

Description:

Hypotension after spinal anesthesia is associated with significant perioperative morbidity and mortality, especially in hypovolemic patients. Ultrasonographic measurement of internal jugular vein (IJV) has been recently shown as effective in predicting the intravascular volume status. The aim was to investigate the reliability of preanesthetic ultrasound measurements of IJV in predicting hypotension after spinal anesthesia.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 47
• Est. completion date: September 24, 2020
• Est. primary completion date: September 24, 2020
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Patients between the ages of 18-65 Patients who read and accept the consent form of the study Patients undergoing elective surgery under spinal anesthesia

Exclusion Criteria:

• under 18 years old, ASA scores 3-4, presence of any significant hepatic, renal, cardiavasculary, or respiratory disease, having left ventricular ejection fraction less than 40%, and allergy to study medications.

Related Conditions & MeSH terms

• Hypotension
• Hypotension Postprocedural
• Spinal Anesthetics Causing Adverse Effects in Therapeutic Use

Intervention

Other:
• spinal anesthesia
prospective observational study

Locations

Country	Name	City	State
Turkey	Eskisehir Osmangazi Univercity	Eskisehir

Sponsors (1)

Lead Sponsor	Collaborator
Eskisehir Osmangazi University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The association between sonographic measurements and postspinal hypotension	The aim of the study is to evaluate the association between sonographic measurements and postinduction hypotension.	first 30 minute