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Opioid requirement between intravenous nalbuphine and morphine for postoperative analgesia after cesarean section under spinal anesthesia

Phase 4
Completed
Conditions
Healthy term pregnant woman
Postoperative pain
Spinal anesthesia
Nalbuphine
Registration Number
TCTR20210903005
Lead Sponsor
/A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
160
Inclusion Criteria

Term pregnancy with
-Age more than18 years
-Patient ASA physical status I-III.
-Scheduled for elective cesarean section under spinal anesthesia
-Can operate a patient-controlled analgesia (PCA) device.

Exclusion Criteria

-Known hypersensitivity to researched drugs
-History of chronic pain
-History of drug addict use
-Patient refuse for spinal anesthesia
-Medical complications eg heart diseases, diabetes, hypertension, renal or hepatic disease, obesity >=100 kilograms
-Gynecological complications eg myoma uteri, ovarian tumors
-Obstetrical complications eg multiple gestation, pre-eclampsia, fetal distress, IUGR(intra-uterine growth retardation), placenta previa

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative morphine and nalbuphine consumption 24 hours milligram
Secondary Outcome Measures
NameTimeMethod
umerical rating scale 6, 12 , 24 hour point,Nausea and vomiting 6,12,24 hour 0-3 point,Pruritus score 6,12,24 hour 0-3 point,Respiratory depression 6 12 24 hour Sedation score 0-3
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