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Recruiting NCT07210892

NCT07210892 Paramedian Incidence Angles in Spinal Anaesthesia

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Clinical Trial Summary
NCT ID NCT07210892
Status Recruiting
Phase
Sponsor Consorci Sanitari de Terrassa
Condition Anesthesia; Adverse Effect, Spinal and Epidural
Study Type OBSERVATIONAL
Enrollment 90 participants
Start Date 2025-09-30
Primary Completion 2026-09-30

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Measurement of needle insertion angles

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 90 participants in total. It began in 2025-09-30 with a primary completion date of 2026-09-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Inclusion Criteria: patients submitted to spinal anaesthesia - Exclusion Criteria: none \-

Contact & Investigator

Central Contact

Anna Puigdellívol-Sánchez, M.D., Ph.D.

✉ apuigdellivol@ub.edu

📞 +34-93-5884555

Principal Investigator

Alberto Prats-Galino, M.D., Ph.D

PRINCIPAL INVESTIGATOR

University of Barcelona

Frequently Asked Questions

Who can join the NCT07210892 clinical trial?

This trial is open to participants of all sexes, studying Anesthesia; Adverse Effect, Spinal and Epidural. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07210892 currently recruiting?

Yes, NCT07210892 is actively recruiting participants. Contact the research team at apuigdellivol@ub.edu for enrollment information.

Where is the NCT07210892 trial being conducted?

This trial is being conducted at Barcelona, Spain.

Who is sponsoring the NCT07210892 clinical trial?

NCT07210892 is sponsored by Consorci Sanitari de Terrassa. The principal investigator is Alberto Prats-Galino, M.D., Ph.D at University of Barcelona. The trial plans to enroll 90 participants.

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