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OpenTrials
Active, Not Recruiting

NCT Number: NCT06948383

SPSIPB vs. SAPB in Breast Surgery

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Conditions

Postoperative Pain Agnosia Nervous System Diseases Neurobehavioral Manifestations Neurologic Manifestations Pain Pain, Postoperative Pathologic Processes Pathological Conditions, Signs and Symptoms Perceptual Disorders Postoperative Complications Quality of Recovery Signs and Symptoms

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Zonguldak Bülent Ecevit University Medicine Faculty

Zonguldak, Kozlu, 67600, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Serratus Posterior Superior Intercostal Plane Block

Procedure

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

Serratus Anterior Plane Block

Procedure

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

Primary outcomes

  1. postoperative opioid consumption

    Time frame: up to 24 hour after surgery

    total opioid consumption during postoperative 24 hours

Secondary outcomes

  1. Postoperative pain scores

    Time frame: postoperative 2nd 6th, 12th 24th hour

    Pain scores evaluate with Numeric rating scale. 0= no pain, 10= unbearable pain

  2. quality of recovery

    Time frame: postoperative 24 hour

    Recovery quality will be measured with Quality of recovery-15 questionnaire

Sponsors and collaborators

Lead sponsor

Zonguldak Bulent Ecevit University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Apr 29, 2025
Registry last updated
Apr 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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