Point-assisted spinal sonography for successful spinal anesthesia

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

TCTR

Registry ID

TCTR20210302007

Enrollment

Registered

2021-03-02

Start date

2020-09-01

Completion date

Unknown

Last updated

2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

none none

Interventions

Point-assisted Spinal Sonography ,pre-procedure ultrasound scan

Experimental Device,Experimental Device

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: aged 18-80 years, BMI under 35, and non-pregnant

Exclusion criteria

Exclusion criteria: pregnant,BMI>35

Design outcomes

Primary

Measure	Time frame
accuracy of the needle insertion point 3 day after intervention number of patient who get CSF from first attempt of spinal anesthesia compare in PASS group and skin marking group	—

Secondary

Measure	Time frame
the duration to achieve the visible CSF one day Mann whitney U test	—

Countries

Thailand

Contacts

Public ContactKetchada Uerpairojkit

Chulalongkorn

ketchada_cc@hotmail.com0896644730

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026