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Comparison of the effect of intravenous Dexamethasone injection with Intrathecal injection On Pain and Nausea and Vomiting of patients undergoing Caesarean sectio

Phase 3
Recruiting
Conditions
Condition 1: Pain. Condition 2: Nausea and Vomiting.
Pain, unspecified
Nausea with vomiting, unspecified
R52.9
R11.2
Registration Number
IRCT20141001019359N16
Lead Sponsor
Bojnourd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
90
Inclusion Criteria

Patient should not have the Absolute contraindications for spinal anesthesia.
The patient should not have a history of previous surgery.
The patient should not have mental and psychological problems and peripheral and central neuropathy.
The patient should not have cardiovascular problems.
ASA I & II
Patients must be vigilant

Exclusion Criteria

Patients who are addictive or have drug abuse.
Patient who has a history of taking beta blockers and Alpha 2-agonists and Calcium Channel Blockers.
For any reason, If we have to perform General Anesthesia after Spinal Anesthesia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain after surgery. Timepoint: During recovery, 30 minutes after surgery and then every 30 minutes until the 2th hour, then at 6, 12 and 24 hours after surgery. Method of measurement: Visual Analog Score (VAS).;Nausea and Vomiting. Timepoint: During recovery, 30 minutes after surgery and then every 30 minutes until the 2th hour, then at 6, 12 and 24 hours after surgery. Method of measurement: Scale for measuring nausea and vomiting.
Secondary Outcome Measures
NameTimeMethod
evel of analgesia. Timepoint: After spinal procedure. Method of measurement: Pin Prink Index.;Duration of analgesia. Timepoint: After the patient leaves the operation room. Method of measurement: Clock.;Hemodynamic parameters. Timepoint: After performing the spinal technique, in the first 15 minutes every 5 minutes and then every 15 minutes until the end of the surgery. Method of measurement: Using the monitoring device.;Medication side effects. Timepoint: From the end of surgery to 24 hours after. Method of measurement: Researcher-made questionnaire.
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