Thoracic

7

Review clinical trials related to Thoracic. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Study to Understand the Utility of the Force Feedback Instruments in Robotic Procedures Using da Vinci 5 Robot

The goal of this observational study is to understand the utility of force feedback instruments in surgeries that are done using the da Vinci 5 robot.

Participants needed: 200
Trial details
Age: 22+Biological sex: AllType: ObservationalSponsor: Intuitive SurgicalUpdated: Feb 25, 2026Locations: 5
Eligibility criteria

Age 22 years or older [+4]

Subject receiving an emergent procedure [+12]

Status: Recruiting

Auricular Acupressure in Prehabilitation

Complementary medicine is recognized for its ability to enhance appetite, increase energy, reduce anxiety, decrease pain, and improve sleep, among many other benefits. Acupuncture is among the most frequent types of complementary medicine practiced in the US, and Medicare currently includes back pain as a reimbursable indication for this therapy. Acupuncture-related therapies may enhance efforts at prehabilitation in candidates for major lung resection.

Participants needed: 40
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: University of ChicagoUpdated: Dec 9, 2025Locations: 1
Eligibility criteria

Being considered for major lung surgery [+9]

Allergy to Vaccaria seeds [+1]

Status: Recruiting

Get Fit for Function

The purpose of this study will be to implement and evaluate a prehab program for pre-frail and frail adults who need to undergo thoracic surgery. The study team hypothesizes using an implementation framework will increase the reach, effectiveness, adoption, and implementation of the prehab program.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ChicagoUpdated: Sep 16, 2025Locations: 1
Eligibility criteria

Age ≥ 18, of any racial or ethnic origin [+2]

Unable to give informed consent [+2]

Status: Recruiting

Improving Thoracic Surgical Care Using Electronic Patient-Reported Outcomes (ePROS)

This is a single-site, non-randomized study on the outcomes of remote real-time "ePRO monitoring" in thoracic surgery patients. ePRO monitoring is a health information technology intervention comprised of delivering longitudinal electronic patient-reported outcome (ePRO) surveys (e.g., on symptoms, and physical functioning) coupled with automated provider alerts for concerning survey responses.

Participants needed: 200
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: UNC Lineberger Comprehensive Cancer CenterUpdated: Aug 7, 2025Locations: 1
Eligibility criteria

18 years or older [+5]

Not completing planned surgery within 3 months of obtaining informed consent [+5]

Status: Recruiting

Frequency and Severity of Respiratory Acidosis During One-lung Ventilation, a Retrospective Pilot Study to Compare Clinician Settings and Those Proposed by the VentilO Application

One-lung ventilation is a mechanical ventilation method frequently used during several thoracic surgeries. One-lung ventilation requires the use of protective ventilation to limit ventilator-induced injury and reduce postoperative respiratory complications. Protective ventilation during one-lung ventilation is specific since tidal volumes are applied by definition to one lung, and it is recommended to use lower tidal volumes, down to 4 ml/kg of ideal body weight. This approach requires individualized ventilation parameters, which differs from the conventional or two-lung ventilation, and there are no clear recommendations regarding respiratory rate adjustment to ensure adequate gas exchange.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Laval UniversityUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Adults (≥ 18 years old) [+2]

Arterial blood gas data unavailable during one-lung ventilation [+1]

Status: Not yet recruiting

Intercostal Nerve Block for Pain Management After Uniportal Video-assisted Thoracoscopic Surgeries

The goal of this clinical trial is to compare the safety and effectiveness of the three intercostal nerve blocks used in pain management in uniportal (one port) thoracoscopic surgeries: internal intercostal nerve blocks (ICNB), external ICNB, and Intercostal catheters. Participants will be randomly assigned to three groups: * First group will undergo internal intercostal nerve block * Second group will be given external intercostal nerve block * Third group will have an intercostal catheter Researchers will compare the three groups to see their impact on post-operative pain management in uniportal VATS.

Participants needed: 90
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Al-Quds UniversityUpdated: Apr 1, 2025Locations: 2
Eligibility criteria

All participants between the ages of 18 and 80 year-old who have elective or urg...

Children - under the age of 18 or participants above the age of 80. [+5]

Status: Recruiting

Rhomboid Intercostal Sub Serratus Plane Block Versus Serratus Anterior Plane Block in Thoractomy

The objective of the current study is to compare the efficacy of the analgesic effect of ultrasound-guided unilateral Rhomboid intercostal and sub serratus plane block (RISS) versus Serratus anterior plane block (SAPB) in Thoracotomy incision.

Participants needed: 40
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Yasser S Mostafa, MDUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

Patients aged 18-70 years. [+4]

ASA PS class ≥ IV patients. [+7]