Spinal anesthesia with Lidocai

Phase 2

• Conditions: Spinal anesthesia.; Local anesthesia

• Registration Number: IRCT201110097745N1
• Lead Sponsor: Vice chancellor for research Kerman University medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Male
• Target Recruitment: 210

Inclusion Criteria

Exclusion criteria:
1 –patients with higher or lower then sixth lumbar vertebrae's primary sensory level of anesthesia
2- Individuals with BMI (Body Mass Index) more than 30 kg/m2 and less than 20 kg/m2
3- Alcohol abusers
4- Patients who refuse spinal anesthesia
5-patients with Less than one year of opium abusers in addicted group
6- Substance abuse in less than 2 last years for patients in non addicted group
7- Substance abusers other than opium
8- Patients who had developed neuropathy formerly or at present

1- Fifteen to sixty five years old men with 150 to 180 centimeters in height
2- Drug addicted individuals with a history of more than one year abuse; specifically those who had shown withdrawal symptoms with abstention of drugs.
3- Patients who didn't use to any narcotic substances in less than 2 last years
** All information is based on the patient's statements.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of spinal anesthesia with Lidocain%5. Timepoint: after 10 minute. Method of measurement: after 10 minute with pinprick on abdomen each 10 minute e %5.

Secondary Outcome Measures

Name	Time	Method
Height. Timepoint: At the time of admit ion. Method of measurement: by patient report.;Age. Timepoint: At the time of admit ion. Method of measurement: by patient report.;Body weight. Timepoint: At the time of admit ion. Method of measurement: by patient report.