Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

New pain block study aims to ease recovery after heart surgery

NCT ID NCT07472296

First seen Mar 17, 2026 · Last updated Jun 23, 2026 · Updated 13 times

Summary

This study compares two regional anesthesia techniques to manage pain in 50 adults undergoing heart surgery via a chest incision. One group receives an Erector Spinae Plane Block, while the other gets a combination of Superficial Parasternal Intercostal Plane Block and Serratus Anterior Plane Block. The goal is to see which method provides better pain control and reduces opioid use.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for CARDIAC SURGERY are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Contacts and locations

Locations

  • Bursa Uludag University Hospital

    RECRUITING

    Bursa, Nilüfer, 16235, Turkey (Türkiye)

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

    Contact Phone: •••-•••-•••• Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Bupivacaine

What this could lead to

If successful, this could point to a better way to manage pain after heart surgery, reducing opioid use and speeding recovery.

What could go wrong

This is a small, early-stage study with only 50 participants, so results may not apply to everyone. The nerve blocks carry risks like infection or bleeding.

Conditions

The condition(s) this trial relates to.

Acute Pain agnosia Pain, Postoperative

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.