Viewing Study NCT05715476



Ignite Creation Date: 2024-05-06 @ 6:36 PM
Last Modification Date: 2024-10-26 @ 2:51 PM
Study NCT ID: NCT05715476
Status: COMPLETED
Last Update Posted: 2024-05-08
First Post: 2022-11-28

Brief Title: The Effect of Different Altitude Levels on Spinal Anesthesia in Cesarean Section Surgery
Sponsor: Giresun University
Organization: Giresun University

Study Overview

Official Title: The Effect of Different Altitude Levels on Spinal Anesthesia in Cesarean Section Surgery Comparison of Anesthesia Parameters and Hemodynamic Changes
Status: COMPLETED
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: altitude
Brief Summary: The aim of the researchers in this prospective study is to determine the differences if any in terms of anesthetic parameters among pregnant women who live at different altitudes and undergo cesarean section under neuraxial anesthesia under elective conditions and to contribute to the literature
Detailed Description: Increased intra-abdominal pressure during pregnancy increases the pressure in the epidural and spinal space and causes enlargement of the epidural veins This may lead to easier increases in the anesthetic blockage level For this reason it is necessary to use the lowest possible dose of local anesthesia in these individuals compared to normal healthy individuals

The literature on the effect of altitude difference on central neuraxial block is limited Based on studies showing changes in CSF volume and content in hypoxic conditions According to the researchers with the same amount of local anesthetic the duration of sensory and motor blockade at sea level is thought to be equal to or longer than in mid-high regions

This study will be carried out among pregnant women who live in the city center at 3 different altitudes 0-10 m Giresun 810 m Çorum 1725 m Van and undergo cesarean section under elective conditions It will be performed in a multicenter prospective controlled randomized manner in order to determine the differences if any among these pregnant women in terms of anesthetic parameters

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None