Cardiac Surgery With Sternotomy

2

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

Condition / disease
Location
Status: Not yet recruiting

Effect of Positioning and ACBT on Pulmonary Complications After Cardiac Surgery

The goal of this quasi-experimental clinical trial is to learn if position management combined with the Active Cycle of Breathing Techniques (ACBT) works to reduce postoperative pulmonary complications in adult patients undergoing elective cardiac surgery. It will also evaluate the individual effects of each technique compared to routine care. The main questions it aims to answer are: Does the combination of positioning and ACBT significantly lower the incidence and severity of postoperative pulmonary complications (like atelectasis, pneumonia, and respiratory failure) within the first 7 days after surgery? Does the combination of these techniques reduce the length of hospital stay compared to using each technique alone or routine care? Does the application of ACBT alone lower the rate of respiratory infections? Does position management alone improve oxygenation parameters (such as SpO\_{2} and PaO\_{2})? Researchers will compare four groups of patients to determine the most effective nursing approach: Group 1 (Control Group): Participants will receive routine postoperative hospital care only. Group 2 (ACBT Group): Participants will perform the Active Cycle of Breathing Techniques (breathing control, thoracic expansion, and huffing) three times daily for 10-15 minutes over 5 postoperative days. Group 3 (Positioning Group): Participants will receive structured position management exclusively, shifting from head elevation (30-45) early after surgery to a semi-recumbent position (approx60) during waking hours, alongside other positions like lateral or forward-leaning as tolerated. Group 4 (Combined Group): Participants will receive both structured position management and perform the ACBT sessions according to the same schedules. All participants will undergo daily respiratory assessments using a standardized scoring system for 7 days post-surgery or until hospital discharge.

Participants needed: 124
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Assiut UniversityUpdated: May 28, 2026Locations: 1
Eligibility criteria

Adult patients (aged from 20 years to 65 years old). [+3]

• Patients undergoing emergency cardiac surgery. [+6]

Status: Recruiting

Suzetrigine-enhanced MultimOdal Opioid-sparing THerapy in Cardiac and Bariatric SURGery

This is prospective, randomized study. The purpose of this study is to evaluate whether the addition of Suzetrigine to well established multimodal pain regimen for participants undergoing bariatric patients undergoing weight-loss surgery and cardiac patients undergoing sternotomy will reduce post-operative opioid consumption and pain scores.

Participants needed: 235
Trial details
Phase: Phase 3Age: 18-85Biological sex: AllType: InterventionalSponsor: Icahn School of Medicine at Mount SinaiUpdated: May 14, 2026Locations: 1
Eligibility criteria

Adults 18-85 years old [+2]

ASA Class V [+8]