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? Comparison effect of addition of Dexmedetomidine and Fentanyl to ?Lidocaine 5% in spinal anesthesia in ?women candidate elective ?cesarea

Not Applicable
Conditions
Elective cesarean.
Delivery by elective caesarean section
Registration Number
IRCT2017012320258N28
Lead Sponsor
Vice chancellor for Research, Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
84
Inclusion Criteria

18 to 35 years; single pregnancy; candidate ?cesarean with spinal anesthesia; elective ?cesarean.
Exclusion criteria: multiple pregnancy; allergy for Fentanyl and dexmedetomidine; infection in site of spinal anesthesia; lack of consent.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Every 5 minute to recovery. Method of measurement: millimeter Hg.;Heart rate. Timepoint: every 5 minute to recovery. Method of measurement: Beat in minute.;Oxygen saturation. Timepoint: every 15 minute to recovery. Method of measurement: Percent.;Breathing. Timepoint: Every 15 minute to recovery. Method of measurement: Number in minute.;Pain. Timepoint: In recovery and 4 and 12 and 24 hours after cesarean. Method of measurement: Visual Analogue Scale.;Duration of analgesia. Timepoint: requesting the first analgesic drug ?. Method of measurement: Miligeram.;Narcotic drug. Timepoint: 24 hours after cesarean. Method of measurement: Miligeram.
Secondary Outcome Measures
NameTimeMethod
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