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Comparison of Early Postoperative Outcomes Between Minimally Invasive Valve Surgery Via Right Thoracotomy and Conventional Valve Surgery Via Sternotomy.

Comparison of Early Postoperative Outcomes Between Minimally Invasive Valve Surgery Via Right Thoracotomy and Conventional Valve Surgery Via Sternotomy

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07251660
Enrollment
32
Registered
2025-11-26
Start date
2025-12-15
Completion date
2026-08-15
Last updated
2025-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Valve Insufficiency, Aortic Valve Stenosis, Heart Valve Diseases or Prosthesis, Valvular Heart Disease Stenosis and Regurgitation (Diagnosis)

Keywords

Heart valve disease, Mitral valve surgery Aortic valve surgery Minimally invasive cardiac surgery, Conventional open-heart surgery, Aortic cross-clamping, Early postoperative outcomes

Brief summary

This randomized controlled trial aims to compare early postoperative outcomes between Minimally Invasive Valve Surgery (MIVS) via right thoracotomy and Conventional Valve Surgery via median sternotomy in patients undergoing elective, isolated mitral or aortic valve surgery. Minimally invasive techniques are believed to reduce postoperative pain, ventilation time, chest drain output, and wound complications, but evidence from Pakistan is limited. The study will enroll patients of all ages and genders who are scheduled for isolated valvular procedures at Chaudhary Pervaiz Elahi Institute of Cardiology (CPEIC), Multan. Participants will be randomly assigned to undergo either minimally invasive thoracotomy or conventional sternotomy. Primary outcomes include ventilation time, CPB duration, cross-clamp time, pain scores, and chest drain output. Secondary outcomes include wound healing (Day 7 and 30 days), return to routine activity, echocardiographic evaluation, transfusion requirements, and 30-day mortality. Findings from this study may provide evidence to guide the adoption of minimally invasive valvular surgery techniques in low-resource and developing settings.

Detailed description

Valvular heart disease is a significant contributor to cardiovascular morbidity worldwide and often requires surgical intervention. Although median sternotomy provides excellent exposure for valve repair and replacement, it is associated with increased surgical trauma, prolonged recovery time, higher postoperative pain, and cosmetically visible scarring. Minimally Invasive Valve Surgery (MIVS) through a right thoracotomy has emerged as a promising alternative approach, offering advantages such as smaller incisions, reduced postoperative discomfort, shorter hospitalization, and improved cosmetic outcomes-without compromising procedural safety. International evidence demonstrates comparable mortality and valve repair quality between the two techniques, with additional benefits favoring minimally invasive approaches such as reduced transfusion needs and fewer sternal wound complications. However, data from Pakistan remain sparse. This randomized controlled trial is designed to evaluate the early postoperative outcomes of MIVS versus conventional sternotomy in a tertiary cardiac surgery center in Pakistan. Eligible patients undergoing elective, isolated mitral or aortic valve surgery will be randomized using a computer-generated sequence to one of two groups: Group A (MIVS): Right anterolateral thoracotomy with femoral cannulation and transthoracic aortic clamping. Group B (Sternotomy): Median sternotomy with standard central cannulation. Both groups will receive standardized anesthesia, cardiopulmonary bypass protocols, myocardial protection strategies, and postoperative ICU care. The surgical procedures will be performed by experienced cardiac surgeons, and all perioperative variables will be recorded using a structured proforma. Primary Outcomes Cardiopulmonary bypass (CPB) time Aortic cross-clamp time Duration of mechanical ventilation Postoperative pain score (NRS at 12 and 24 hours) Total chest drain output in the first 24 hours Secondary Outcomes PRBC transfusion requirement Wound condition on postoperative day 7 Echocardiographic findings before discharge and at 30 days Return to routine daily activity by 30 days 30-day all-cause mortality Patients will be followed for 30 days after surgery. Data will be analyzed using IBM SPSS v25. Continuous variables will be compared using an independent samples t-test, while categorical variables will be assessed via the Chi-square test. A p-value of \<0.05 will be considered statistically significant. This study aims to provide local evidence comparing the two surgical approaches and help determine whether minimally invasive valve surgery should be more widely adopted as a preferred option in tertiary cardiac surgical practice.

Interventions

PROCEDUREMinimally Invasive Valve Surgery

Participants in this group will undergo minimally invasive valve surgery through a right anterolateral thoracotomy. A small 5-7 cm incision will be made in the 4th or 5th intercostal space. Cardiopulmonary bypass will be established using femoral arterial and venous cannulation. A transthoracic aortic cross-clamp will be applied, and cold blood cardioplegia will be administered. The mitral or aortic valve will be accessed through limited thoracic exposure and repaired or replaced using standard techniques. This approach avoids median sternotomy and aims to reduce postoperative pain, ventilation time, transfusion needs, and wound complications.

PROCEDUREConventional Valve Surgery

Participants in this group will undergo conventional open-heart valve surgery through a full median sternotomy. Cardiopulmonary bypass will be established using aortic and right atrial cannulation. Standard antegrade cold blood cardioplegia will be administered for myocardial protection. The mitral or aortic valve will be exposed through full sternal access and repaired or replaced following established institutional protocols. This approach represents the traditional surgical method used for valvular heart disease.

Sponsors

Chaudhry Pervaiz Elahi Institute of Cardiology
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients of any age and gender. * Undergoing elective, isolated mitral or aortic valve surgery. * Considered suitable for either: * MIVS via right thoracotomy, or * Conventional valve surgery , as decided by the operating surgical team. * Patients giving written informed consent.

Exclusion criteria

* Emergency or redo cardiac surgeries * Concomitant cardiac procedures (e.g., CABG, multiple valve replacements) * Ejection Fraction \<30% * Severe pulmonary hypertension (identified as the mean pulmonary artery pressure (mPAP) exceeding 45 mmHg on echocardiography, as outlined by the AHA guidelines(10). * Active systemic infections or sepsis at the time of surgery * Refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Duration of Mechanical Ventilation24 hoursThe duration of postoperative mechanical ventilation will be measured in hours from the time the patient arrives in the intensive care unit (ICU) after surgery until successful extubation. This outcome evaluates early recovery, respiratory function, and perioperative morbidity following minimally invasive valve surgery versus conventional sternotomy.

Secondary

MeasureTime frameDescription
Aortic Cross-Clamp TimeDuring surgeryTotal duration in minutes during which the aorta is cross-clamped during cardioplegic arrest. This outcome assesses technical complexity and myocardial protection demands in each surgical approach.
Chest Drain OutputFirst 24 hours postoperativelyTotal volume of mediastinal and pleural drainage collected in the first 24 hours after surgery, measured in milliliters. This evaluates postoperative bleeding and tissue trauma associated with each surgical technique.
Postoperative Pain Score (NRS)12 hours and 24 hours after surgeryPain intensity measured using the Numeric Rating Scale (0-10) at 12 hours and 24 hours postoperatively, assessing the effect of surgical access on postoperative comfort and recovery.
Cardiopulmonary Bypass TimeDuring surgeryTotal duration of cardiopulmonary bypass (CPB) measured in minutes from initiation to termination of bypass during surgery. This evaluates intraoperative efficiency and the impact of minimally invasive versus conventional surgical access on operative time.
SSI at 30-Day Follow-Up30 days postoperativelyEvaluation of wound healing and complications at 30 days after surgery, including infection, dehiscence, or healthy healing, assessed during outpatient follow-up.
Packed Red Blood Cell Transfusion RequirementFirst 24 hours postoperativelyNumber of units of packed red blood cells transfused within the first 24 hours after surgery, recorded to compare postoperative bleeding and transfusion needs.
30-Day All-Cause MortalityWithin 30 days postoperativeMortality due to any cause occurring within 30 days after surgery, including in-hospital or post-discharge events verified through medical records or contact with the patient's family.
SSI on Postoperative Day 7Postoperative day 7Assessment of the surgical wound for signs of erythema, discharge, infection, or dehiscence, classified as healthy or infected. This evaluates early wound healing differences between thoracotomy and sternotomy.

Contacts

Primary ContactDr Bilal Hassan Resident Cardiac Surgery, MBBS
garhamore88@gmail.com+3006157734
Backup ContactMuhammad Hamid Senior Registrar, MBBS
dr.hamid632@gmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026