Clinical trial Recruiting at 1 site Observational Ages 18 and up

SPSIP Block in Shoulder Arthroscopy (Observational)

Official title: Clinical Effectiveness of the Serratus Posterior Superior Intercostal Plane Block (SPSIP Block) in Shoulder Arthroscopy: an Exploratory Prospective Observational Study

Run by ULSS6 - Ospedale di Piove di Sacco · NCT07874672 · Data updated 2026-11-12

This study tests how the SPSIP block affects sensory feeling and shoulder movement during shoulder arthroscopy in adults.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment20 (estimated)
SponsorULSS6 - Ospedale di Piove di Sacco
Academic / other
Locations1 site (Piove di Sacco, Padova)
StatusRecruiting
StartedOctober 14, 2026
Main results expectedJanuary 2027
Study endsMarch 2027
Registry record updatedOctober 21, 2026
Trial IDNCT07874672 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults undergoing shoulder arthroscopy for whom the anesthesiologist has chosen an SPSIP block and who can give informed consent.

Probably not a fit

Patients with pre-existing neuropathies or those not receiving SPSIP block may not benefit from this observational description.

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

What this trial studies

This is a prospective, single-center observational study in Italy that describes sensory blockade after SPSIP blocks used for shoulder arthroscopy. Researchers map changes in sensation on the shoulder area 30 minutes after the block and assess upper-limb motor function and diaphragmatic movement. Data collected include patient demographics, block details, sensory mapping using cold sensation, and range-of-motion measurements. The study does not alter anesthesia management and uses routine care procedures. The goal is to understand the sensory coverage and potential motor and diaphragmatic sparing of the SPSIP approach.

Why it matters

Potential benefit: If successful, the SPSIP block could provide effective shoulder pain relief with less motor impairment and diaphragmatic involvement.

How similar studies have gone: Other studies have suggested the SPSIP block may spare motor function compared with brachial plexus blocks, but systematic descriptions of its sensory and diaphragmatic effects remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patients scheduled for shoulder arthroscopy receiving an SPSIP block as the analgesic technique.
* Age ≥ 18 years.
* Patients able to provide informed consent to study participation and to the processing of personal data.

Exclusion Criteria:

* Refusal to provide consent to study participation.
* Pre-existing central or peripheral sensory neuropathy.
* Estimated time between block performance and entry into the operating room of less than 30 minutes.

Where it's running

  • Ospedale di Piove di Sacco
    Piove di Sacco, Padova, 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.