New nerve block could ease pain after Open-Heart surgery
NCT ID NCT07232992
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a nerve block called SPSIPB to see if it reduces pain and opioid use after open-heart surgery. 70 adults were randomly assigned to receive either the SPSIPB or standard pain management. The goal was to compare pain scores and recovery over 24 hours.
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 effective, this nerve block could offer better pain relief and faster recovery after open-heart surgery, reducing the need for strong painkillers.
- What could go wrong
- This is a small, completed trial with 70 patients, so results may not apply to everyone. The block may not work better than current methods, and there are risks like allergic reactions or nerve damage.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
70 people
The number who actually took part.
- Started
-
Jan 2026
- Finished
-
Apr 2026
- Lead sponsor
-
A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 85 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged 18-85 years with ASA physical status II-III undergoing elective open-heart surgery. Exclusion Criteria: Patients who do not consent to participate in the study Patients with coagulopathy History of allergy or toxicity to local anesthetics Patients with hepatic or renal failure Patients with uncontrolled diabetes mellitus Patients with uncontrolled hypertension Mentally disabled patients Patients receiving chronic pain therapy (opioid use) Use of antidepressant medication Presence of neuropathic pain Presence of infection at the injection site Pregnant, suspected pregnant, or breastfeeding women
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Bursa City Hospital
Bursa, Turkey (Türkiye)
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