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SPSIPB vs. SAPB in Breast Surgery

Serratus Posterior Superior Intercostal Plane Block Versus Serratus Anterior Plane Block for Breast Surgery: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06948383
Enrollment
90
Registered
2025-04-29
Start date
2025-04-01
Completion date
2025-10-01
Last updated
2025-04-29

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

Conditions

Postoperative Pain, Quality of Recovery

Keywords

postoperative pain, pain scores, Pain management, Fasial plane blocks

Brief summary

The effects of the newly defined serratus posterior superior intercostal plane block and serratus anterior plane block on postoperative analgesia and quality of recovery in women undergoing breast surgery will be investigated.

Interventions

PROCEDURESerratus Posterior Superior Intercostal Plane Block

administer 30 mL %0.25 bupivacain between third costa and serratus posterior superior muscle

PROCEDURESerratus Anterior Plane Block

administer 30 mL %0.25 bupivacain between 5th costa and serratus anterior muscle in midaxiller line

Sponsors

Zonguldak Bulent Ecevit University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients who have received informed consent form Patients who will undergo Breast Cancer Surgery aged between 18-65

Exclusion criteria

* \<18 years and \>65 years * ASA ≥ IV * History of allergy to local anesthetics * Clinical diagnosis of coagulation disorders * Infection near the entry site * Chronic analgesic use Patients who will undergo bilateral Breast Cancer Surgery * Body mass index \>35 * Clinical diagnosis of Dementia or confusion * Lack of cooperation

Design outcomes

Primary

MeasureTime frameDescription
postoperative opioid consumptionup to 24 hour after surgerytotal opioid consumption during postoperative 24 hours

Secondary

MeasureTime frameDescription
Postoperative pain scorespostoperative 2nd 6th, 12th 24th hourPain scores evaluate with Numeric rating scale. 0= no pain, 10= unbearable pain
quality of recoverypostoperative 24 hourRecovery quality will be measured with Quality of recovery-15 questionnaire

Countries

Turkey (Türkiye)

Outcome results

None listed

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