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Effect of Mexiletine on spinal anesthesia with lidocaine

Evaluation of Mexiletine effect on duration of sensory and motor block in spinal anesthesia with lidocaine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201210077488N4
Enrollment
60
Registered
2012-11-02
Start date
2012-06-21
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

Anesthesia. Injuries to the knee and lower leg

Interventions

Intervention 1: Intervation group received oral mexiletine 200 mg 2 hours before operation. Intervention 2: Control group ricieved multivitamin capsul 2 hours before operation.
Treatment - Drugs
Intervation group received oral mexiletine 200 mg 2 hours before operation
Control group ricieved multivitamin capsul 2 hours before operation

Sponsors

Kerman University of Medical Science( Research and Technology center)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria;Elective lower limb surgery; Age 18-51years;Height 150-190cm; Weight 50-90kg;ASA 1,2 Exclusion criteria; ??Alchohole or narcotic drug consumption;Psychological disorders;Allergic reaction with lidocaine;Infection wound ;Open lower limb fracture;Liver disease;Bradycardia;Cardiac block;Seizure;Recieve analgesic or opiuom before operation .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration time of sensory block. Timepoint: Every 10 min. Method of measurement: The onset time from not sensing pin prick at T10 dermatom until two dermatoms regression from T10.;Duration time of motor block. Timepoint: Every 10 min. Method of measurement: The onset time from unabling to elevate knee until flexion of leg.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sharifzadeh Mahdieh

Kerman University of Medical science

M H Zamanin 680 @ Yahoo.com+98 34 1222 8034

Outcome results

None listed

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