Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating cold sensitivity after a thoracic ESP block in breast cancer surgery

Official title: Evaluation of the Onset and the Extent of Sensory Block After Thoracic ESP Block in Breast Surgery - a Prospective Observational Study

Run by Ospedale Santa Maria Goretti · NCT06642142 · Data updated 2026-11-12

This study is testing how quickly a pain relief technique used during breast cancer surgery affects cold sensitivity in patients.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorOspedale Santa Maria Goretti
Academic / other
Locations1 site (Latina, Italy)
StatusRecruiting
StartedNovember 7, 2024
Main results expectedOctober 2025
Study endsOctober 2025
Registry record updatedNovember 8, 2024
Trial IDNCT06642142 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adult patients aged 18 and older scheduled for breast surgery who meet specific health criteria.

Probably not a fit

Patients with allergies to local anesthetics or those with significant comorbidities may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the onset of sensory block and changes in cold sensitivity following a thoracic erector spinae plane (ESP) block in patients undergoing breast cancer surgery. The procedure involves administering a local anesthetic at the T4 level using an ultrasound-guided technique before surgery. Patients will be monitored for cold sensitivity at specified intervals up to 40 minutes after the block. The study focuses on understanding how quickly the anesthetic spreads and its effectiveness in providing analgesia during surgery.

Why it matters

Potential benefit: If successful, this study could improve pain management strategies for patients undergoing breast cancer surgery.

How similar studies have gone: While this approach is observational, similar techniques have shown promise in improving analgesia in surgical settings, suggesting potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years.
* ASA score I-II-III.
* Schedule of breast surgery
* Schedule of ESPB
* Consent to the study

Exclusion Criteria:

* Allergy to local anaesthetics
* Cardiopathies, nephropathies, hepatopathies, central or peripheral neuropathies uncompensated
* Infection at the injection site
* Uncooperative patient
* BMI \< 20, \> 40
* Difficulty in visualising target structures or the LA spread (failure of technique)
* Pregnancy status

Where it's running

  • Ospedale Santa Maria Goretti, Via Lucia Scaravelli
    Latina, Italy, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.