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Evaluating the effects of using an ancillary method for performing lumbar puncture

Randomized clinical trial of comparing the results of routine lumbar puncture (LP) and ultrasound assisted lumbar puncture via emergency physicians in patients referring to emergency department

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013102511067N3
Enrollment
50
Registered
2013-11-06
Start date
2013-09-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Lumbar puncture. Postprocedural disorders of nervous system, not elsewhere classified

Interventions

Intervention 1: In intervention group, route for lumbar puncture will be defined and confirmed by using ultrasound. Intervention 2: In control group, lumbar puncture will be performed as routine.
Diagnosis
In intervention group, route for lumbar puncture will be defined and confirmed by using ultrasound.
In control group, lumbar puncture will be performed as routine.

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 149 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Being more than 18 years old; need to perform a lumbar puncture for definite diagnosis of disease. Exclusion criteria: Contraindications for lumbar puncture such as infections in the site, spinal vertebrae malformations and surgeries on vertebrae.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Time to perform the procedure. Timepoint: At the end of procedure. Method of measurement: By performer of the procedure.;Number of tries to perform a successful procedure. Timepoint: At the end of procedure. Method of measurement: By performer of the procedure.;Success rate. Timepoint: At the end of study. Method of measurement: By performer of the procedure.;Rate of drytap. Timepoint: At the end of study. Method of measurement: By performer of the procedure.

Secondary

MeasureTime frame
Cerebrospinal fluid leak. Timepoint: At the end of procedure and at the end of study. Method of measurement: By performer of the procedure.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Moloud Balafar

Tabriz University of Medical Sciences

mbalafar@yahoo.com+98 41 1334 1317

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026