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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03740399
Other study ID # TÜTF-BAEK 2018/79
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
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
Health authority
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

Study Design


Related Conditions & MeSH terms


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
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