Clinical Trials Directory

Trials / Completed

CompletedNCT05332379

Regional Hemodynamic Parameter Changes After Spinal Anesthesia

Measurement of Regional Hemodynamic Parameters Before and After Spinal Anesthesia with Doppler USG

Status
Completed
Phase
Study type
Observational
Enrollment
35 (actual)
Sponsor
Marmara University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Spinal anesthesia is a regional anesthesia method used for surgical procedures generally involving the lower abdominal area, perineum, and lower extremities. Various tests are performed to evaluate the block level after spinal anesthesia, incluyding pinprick test, cold application, and motor examination. These tests are performed to check whether the pain, sympathetic and motor nerve fibers are affected, respectively, after the block; and good communication with the patient is important here. However, it is extremely difficult to evaluate these tests in pediatric, geriatric, mentally retarded or uncooperative patients. Sympathectomy can be used as a criterion to evaluate the success of the block that occurs after the spinal anesthesia procedure. Sympathetic nerve fibers are the first to be affected by the block, and the success of the block can be evaluated with the revealed sympathectomy. Sympathectomy in the lower extremities after spinal block increases arterial blood flow. This increase in blood flow can be detected by the Pulsed Wave Doppler feature of USG.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTPulsed Wave Doppler USG examinationPulsed Wave Doppler USG examination of the posterior tibial artery on the left or right lower extremity will be performed before spinal anesthesia, at the 5th and 10th minutes after the spinal anesthesia. Blood flow velocities and vessel diameters will be measured.

Timeline

Start date
2022-04-01
Primary completion
2023-07-20
Completion
2023-07-20
First posted
2022-04-18
Last updated
2024-12-31

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05332379. Inclusion in this directory is not an endorsement.