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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03740399
Acronym
cesarean
Enrollment
180
Registered
2018-11-14
Start date
2018-04-19
Completion date
2019-06-28
Last updated
2018-11-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Regional Anesthesia Morbidity

Keywords

sitting position, lateral decubitus position, spinal block

Brief 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.

Detailed 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.

Interventions

PROCEDUREspinal anesthesia

Investigators will perform spinal anesthesia for section

Sponsors

Trakya University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
spinal anesthesia successspinal anesthesia success will be 15 minutes in intraoperativeThe free flow of clear cerebrospinal fluid (CSF) upon first attempt was considered to be evidence of a successful LP.

Countries

Turkey (Türkiye)

Contacts

Primary ContactSevtap Hekimoglu Sahin, Professor
sevtaphekimoglu@mynet.com+90-284-235-76-41
Backup ContactBeyhan Karamanlıoglu
beykar@mynet.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026