Effect of Modified 45-degree Head-up Tilt Position in Cesarean Operation to the Success of Spinal Anesthesia

Regional Anesthesia Morbidity Clinical Trial

— cesarean  

Official title:

Effect of Modified 45-degree Head-up Tilt Position in Cesarean Operation to the Success of Spinal Anesthesia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03740399
• Other study ID #: TÜTF-BAEK 2018/79
• Status: Recruiting
• Phase: N/A
• Start date: April 19, 2018
• Est. completion date: June 28, 2019

Study information

• Verified date: November 2018
• Source: Trakya University
• Contact: Sevtap Hekimoglu Sahin, Professor
• Phone: +90-284-235-76-41
• Email: sevtaphekimoglu[@]mynet.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The success of the application of spinal block in 3 different application as the sitting position, side decubitus position and 45 degrees head upside side decubitus position will be evaluated.

Description:

180 patients in ASA I-II risk group between the ages of 18-50 will be included in the study.The success of the application of spinal block in 3 different application as the sitting position, side decubitus position and 45 degrees head upside side decubitus position will be evaluated. Anatomical features of height, weight, block application of the patients will be recorded.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 180
• Est. completion date: June 28, 2019
• Est. primary completion date: March 28, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• caesarean section

• 18-50 years old

• ASA I-II risk

Exclusion Criteria:

• heart failure

• patient's refusal

• thrombocytopenia

• coagulation disorder

• heart valve diseases

Related Conditions & MeSH terms

• Regional Anesthesia Morbidity

Intervention

Procedure:
• spinal anesthesia
Investigators will perform spinal anesthesia for section

Locations

Country	Name	City	State
Turkey	Trakya University	Edirne	Centrum

Sponsors (1)

Lead Sponsor	Collaborator
Trakya University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	spinal anesthesia success	The free flow of clear cerebrospinal fluid (CSF) upon first attempt was considered to be evidence of a successful LP.	spinal anesthesia success will be 15 minutes in intraoperative