Paramedian Incidence Angles in Spinal Anaesthesia

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorConsorci Sanitari de Terrassa

About this trial

The objective here is to quantify the number of punctures and redirections during routine practice in the anesthesiology department, verify the final angle of incidence and the sac-skin distance by ultrasound, and determine the optimal, maximum, and minimum angles that would have allowed successful punctures. The objective is also to correlate ultrasound and plain X-ray distances, if available. These angles would then be inferred in advance in patients who must undergo spinal anesthesia, assessing whether this prior estimate reduces the number of punctures and redirections.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Any patients requiring spinal anaesthesia

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Measurement of needle insertion angles

    Other intervention

    Individualization of needle insertion angle depending on the skin to dural sac distance by means of visual guides and adapted protractors

Treatment groups

90 Participants
are divided into 1 treatment group
Group A: Phase 1. Observational1 intervention

Trial outcomes

Primary outcomes

1

Number of needle insertion attempts

Total number of times that the spinal needle is introduced in the skin

Time frame
From September 2025 to september 2026.

Secondary outcomes

1

Number of needle redirections

Total number of needle redirections in all insertion attempts in a single patient.

Time frame
From september 2025 to september 2028

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Consorci Sanitari de Terrassa

Lead sponsor

University of Barcelona

Sponsor institution

University of Barcelona

Collaborator

Hospital Clinic of Barcelona

Collaborator