MedPath

morphine plus Naloxone in cesaria

Phase 3
Recruiting
Conditions
cesarean.
Encounter for cesarean delivery without indication
Registration Number
IRCT20140524017811N8
Lead Sponsor
Sari University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
60
Inclusion Criteria

patents admit in Emam hospital For cesarian
ASA classification 1or 2
60 -80 Kg weight
first or second pregnancy

Exclusion Criteria

Patients who used opiate drugs before cesarean section
consumption of any medicine to reduce itching
unsuccessful spinal anesthesia
prolong surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: The pain level will be evaluated at 2, 4, 6 and after 24 hours after surgery. Method of measurement: Visual Analogue Scale(VAS).
Secondary Outcome Measures
NameTimeMethod
ausia. Timepoint: it will be evaluated at 2, 4, 6 and 24 hours after surgery. Method of measurement: asking the patient.;Itching. Timepoint: will be evaluated at 2, 4, 6 hours after surgery. Method of measurement: asking the patient.
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