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Search / Trial NCT06908681

Intertransverse Process Block for Postoperative Acute Pain After Coronary Bypass Surgery

Launched by MUSTAFA AYDEMIR · Mar 27, 2025

Trial Information

Current as of September 25, 2025

Recruiting

Keywords

Intertransverse Process Block Coronary Artery Bypass Grafting Postoperative Pain Cardiac Surgery Median Sternotomy

ClinConnect Summary

This clinical trial is studying a method called bilateral intertransverse process block (ITPB) to see if it can help reduce pain after coronary artery bypass grafting (CABG) surgery, which is a common heart surgery. In this trial, patients who are scheduled for this surgery will be randomly chosen to receive either the ITPB treatment or a placebo (a harmless saltwater injection) before their operation. The researchers will then monitor how much pain the patients feel after the surgery, how much pain medicine they need, and how well they recover during the first 24 hours after waking up from anesthesia.

To participate in this study, patients must be at least 18 years old and have planned, non-emergency CABG surgery. They should be able to give their consent and communicate their symptoms clearly to the research team. However, individuals with certain conditions, like those requiring emergency surgery or having infections at the injection site, will not be eligible. If you’re interested in this trial, it’s important to know that it’s not yet recruiting participants, but it aims to help improve pain management for heart surgery patients in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age ≥ 18 years
  • Elective coronary artery bypass grafting (CABG) via median sternotomy planned
  • Able to provide written informed consent
  • Able to communicate symptoms reliably with the research team
  • Exclusion Criteria:
  • Emergency CABG surgery
  • Infection or open wound at the injection site
  • Coagulopathy
  • Hepatic or renal failure
  • Reoperation cases
  • Incomplete or missing data

About Mustafa Aydemir

Mustafa Aydemir is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and evidence-based practices, he leads initiatives that bridge the gap between scientific discovery and clinical application. Mustafa's extensive experience in trial design, regulatory compliance, and patient engagement ensures that studies are conducted efficiently and ethically. His collaborative approach fosters partnerships with healthcare professionals and research institutions, promoting rigorous investigation and the translation of findings into meaningful healthcare solutions.

Locations

Konya, Turkey

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported