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Comparison of Modified Paramedicine Spinal Anesthesia with Classic Paramedin

Spinal anesthesia with modified paramedian approach:copmarision with classic paramedian approach

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180518039700N2
Enrollment
200
Registered
2020-08-06
Start date
2020-06-30
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Comparison of spinal anesthesia Paramedin modified paralysis and classical paramedin. Other complications of anesthesia

Interventions

Intervention 1: Intervention group:In this group,anesthesiologist in a sitting position from the L3-L4 or L4-L5 space with the spinal needle with the thumb, the outer margin of the multifidus muscle,

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: All patients aged 20 to 60 years are candidates for spinal anesthesia with ASA rating,grade 1&2. Body mass index less than 30

Exclusion criteria

Exclusion criteria: Visible spinal deformity History of chronic or acute headache Emergency surgery Weight over 100 kg and height less than 50 Surgery more than 3 hours

Design outcomes

Primary

MeasureTime frame
Time to reach the successful block. Timepoint: From the start of the block attempt to the result. Method of measurement: In minutes.;Patient satisfaction with the procedure. Timepoint: After the operation. Method of measurement: Depending on the patient's questions (very low, low, high, very high).;The comfort level of the anesthesiologist regarding the experience of the two techniques Paramedic Classic and Modified. Timepoint: After the operation. Method of measurement: Question from anesthesiologist (easier, more difficult, indifferent).;Feeling of back pain while performing the procedure. Timepoint: From the beginning of the procedure to the end of the work. Method of measurement: Patient's own statements (no, mild, moderate, severe).

Secondary

MeasureTime frame
Headache after the block. Timepoint: 6,12,24, 48 hours after the operation. Method of measurement: Patient's own statements (no, mild, moderate, severe).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSolmaz Fakhari

Tabriz University of Medical Sciences

solmaz_fakhari@yahoo.com+98 41 3334 1994

Outcome results

None listed

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