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The effect of Intrathecal Atropine to prevent Nausea & Vomiting after surgeries due to use Intrathecal Morphine in lower limb surgeries

Phase 2
Conditions
Spinal Anesthesia.
local anaesthetics
Registration Number
IRCT2013012012204N1
Lead Sponsor
Vice chancellor for research, Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
Inclusion Criteria

Participants including major eligibility criteria:
The patients aged from 40-70 years
Participants excluding major eligibility criteria:
Patients with history Neurologic disease and Neuromuscular; Diabetes Mellitus; Patients with Neuropathy Peripheral; Infection in site of injection; Sensitivity to Local Anesthesia; Patients with Vomiting and Nausea before surgery or receiving 48 hours before surgery Anti Vomiting and Nausea; Women in period of mense

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of Vomiting and Nausea. Timepoint: Incidence of Nausea and Vomiting were studied in patients within 24 hours after injection of Atropine: Hourly up to 6 hours, Then 6 hours later and Finally 12 hours later. Method of measurement: With checklist: Mild; Moderate; Severe.
Secondary Outcome Measures
NameTimeMethod
Heart Rate. Timepoint: 3,5,10,15 Minutes after Spinal Anesthesia with receiving Atropin Interathecal. Method of measurement: Heart Rate per minute.;Blood Pressure. Timepoint: 3,5,10,15 Minutes after Spinal Anesthesia with receiving Atropin Intrathecal. Method of measurement: Blood volume pump by heart.;With out pain period. Timepoint: Intrathecal Morphine-Induced Analgesia was studied in 2 hours intervals for 12 hours after injection. Method of measurement: With checklist.
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