ClinicalTrials.Veeva

Menu

TAPSE/PASP Anesthesia

A

Aydin Adnan Menderes University

Status

Not yet enrolling

Conditions

Hypotension

Treatments

Other: hypotension

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

TAPSE, one of the methods for evaluating right ventricular systolic function; It is a bar parameter that can easily measure apex-basal shortening and provides specific information about global RV function. TAPSE/PASP can be calculated as load-independent parameters to evaluate RV function. Because RV function is sensitive to change in afterload, known as the RV-pulmonary circulation (PC) connection.

This study aims to identify patients who are candidates for hypotensive events due to general anesthesia in a hemodynamically stable population.

Full description

TAPSE, one of the methods for evaluating right ventricular systolic function; It is a bar parameter that can easily measure apex-basal shortening and provides specific information about global RV function. TAPSE/PASP can be calculated as load-independent parameters to evaluate RV function. Because RV function is sensitive to change in afterload, known as the RV-pulmonary circulation (PC) connection.

This study aims to identify patients who are candidates for hypotensive events due to general anesthesia in a hemodynamically stable population.

Patients will be measured by transthoracic echocardiography in the preoperative period, 15-30 minutes before induction.

Basal hemodynamic parameters and non-invasive and/or hemodynamic values will be recorded every two minutes after induction until surgical incision.Patients with a 30% decrease in SBP from the baseline and a decrease in MAP below 65 mmHg in the first 10 minutes after anesthesia induction will be considered to have hypotension. Patients will be divided into 2 groups: 'with' and 'without' hypotension.

Enrollment

52 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Written informed consent;
  2. 18-75 years old
  3. ASA Physical Status 1-3;
  4. Patients planned for pulmonary resection surgery

Exclusion criteria

  1. The patient is pregnant
  2. After cardiac surgery
  3. Severe pulmonary hypertension
  4. Severe valve disease
  5. Hypertrophic or dilated cardiomyopathy
  6. Presence of acute myocardial infarction
  7. Patients with severe visual or hearing impairment/disability
  8. ASA physical status IV or V
  9. Ischemic heart disease, conduction disorder.
  10. History of long-term use of certain medications (β-blockers, angiotensin converting enzyme inhibitors, analgesics, sedatives or tricyclic antidepressants)

Trial design

52 participants in 2 patient groups

Hypotension
Description:
Patients with a 30% decrease in SBP from baseline and a decrease in MAP below 65 mmHg in the first 10 minutes after anesthesia induction will be considered to have hypotension.
Treatment:
Other: hypotension
none hypotension
Description:
Patients who do not have a 30% decrease from the baseline in SBP and a decrease in MAP below 65 mmHg in the first 10 minutes after anesthesia induction will be considered as not having hypotension.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems