← Back to Clinical Trials
Recruiting NCT07577700

NCT07577700 Assessment of Pulmonary Perfusion and Hemodynamic Measurements by Electrical Impedance Tomography in Patients Undergoing Pulmonary Thromboendarterectomy.

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07577700
Status Recruiting
Phase
Sponsor University of Sao Paulo General Hospital
Condition Pulmonary Thromboendarterectomy
Study Type INTERVENTIONAL
Enrollment 36 participants
Start Date 2025-02-25
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Electrical Impedance Tomography (EIT).Pulmonary Perfusion SPECT-CT.Pulmonary Thromboendarterectomy.

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 36 participants in total. It began in 2025-02-25 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Chronic thromboembolic pulmonary hypertension (CTEPH) is a condition in which old blood clots block the blood vessels in the lungs, making it harder for the heart to pump blood through the lungs. Surgery called pulmonary thromboendarterectomy can remove these clots and improve blood flow, but doctors need reliable ways to evaluate lung blood flow before and after surgery. This study will evaluate a bedside imaging method called electrical impedance tomography (EIT), which can measure how blood flows through different regions of the lungs without radiation or invasive procedures. Patients undergoing surgery for CTEPH will be monitored with EIT before and after surgery, and the results will be compared with standard lung perfusion imaging. The goal of this study is to determine whether EIT can provide useful information about lung blood flow and changes after surgery, and whether it could serve as a complementary bedside tool to help monitor patients with CTEPH.

Eligibility Criteria

Inclusion Criteria: \- Patients diagnosed with chronic thromboembolic pulmonary hypertension (CTEPH) followed at the Pulmonology Service of InCor-HCFMUSP and scheduled for pulmonary thromboendarterectomy at InCor-FMUSP. Exclusion Criteria: * Age under 18 years * Pregnancy * Structural heart disease (atrial septal defect, ventricular septal defect, or valvular heart disease) * Cardiac arrhythmias * Use of a cardiac pacemaker or other implantable electronic device * Skin lesions on the thoracic region at the site of EIT electrode belt placement * Absence of central venous access on the day of the preoperative protocol evaluation * Difficulty understanding the procedures to be performed * Refusal to participate in the study (non-signing of the Informed Consent Form) * Refusal by the attending medical team

Contact & Investigator

Central Contact

Marcelo BP Amato, MD PhD

✉ marcelo.amato@hc.fm.usp.br

📞 +55113061-7361

Frequently Asked Questions

Who can join the NCT07577700 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Pulmonary Thromboendarterectomy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07577700 currently recruiting?

Yes, NCT07577700 is actively recruiting participants. Contact the research team at marcelo.amato@hc.fm.usp.br for enrollment information.

Where is the NCT07577700 trial being conducted?

This trial is being conducted at São Paulo, Brazil.

Who is sponsoring the NCT07577700 clinical trial?

NCT07577700 is sponsored by University of Sao Paulo General Hospital. The trial plans to enroll 36 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology