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Completed

NCT Number: NCT06100419

SPSIP Block in Breast Surgeries for Postoperative Analgesia

The aim of this clinical study is to demonstrate that pain following breast surgeries can be reduced through the application of serratus posterior superior intercostal plane block (SPSIPB). Seven patients scheduled for breast surgery were included in the study. The primary research question it seeks to address is as follows: • Can SPSIPB be applied to reduce pain following breast surgeries? Participants are expected to provide accurate responses to the researcher's questions for the assessment of postoperative pain.

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Key information

Conditions

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Sivas Cumhuriyet University

Sivas, 58050, Turkey (Türkiye)

About this study

Postoperative analgesia techniques for breast surgeries encompass options such as Paravertebral Block, Erector Spinae Plane Block, Serratus Anterior Plane Block, and Pectoral Nerve Blocks. Although the Paravertebral Block is considered the gold standard for postmastectomy pain relief, its limited usage is primarily attributed to complications. SPSIPB's potential in thoracic surgeries has been noted, offering a broad sensory block suitable for MRM and axillary lymph node dissection. In this study, the effectiveness of SPSIP block for post-mastectomy pain has been investigated.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Female patients who will undergo breast surgery

Exclusion criteria

  • unstable patients
  • patients with bleeding disorders
  • Patients allergic to local anesthetic drugs
  • Patients who did not agree to participate in the study
  • Patients with infection at the application site

Treatment and study plan

Serratus Posterior Superior Intercostal Plane Block

Procedure

With this newly introduced procedure added to the literature, patients undergoing breast surgeries are expected to experience reduced pain.

Other names: SPSIPB

Primary outcomes

  1. numeric rate scores (NRS)

    Time frame: first 24 hours

    The pain levels of patients are indicated with a number between 1 and 10. its means: 0=no pain, 10=worst pain.

Secondary outcomes

  1. total tramadol consumption

    Time frame: first 24 hours

    The total analgesic quantity that patients will consume for pain reduction.

Sponsors and collaborators

Lead sponsor

Cumhuriyet University

Other

Registry information

Official study title

Is Serratus Posterior Superior Intercostal Plane Block Effective in Modified Radical Mastectomy Surgeries?

Acronym: SPSIPB

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Oct 25, 2023
Registry last updated
Oct 26, 2023

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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