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The efficacy of preemptive gabapentin for pain reduction after gynecologic surgery

Phase 4
Completed
Conditions
Preemptive gabapentin 600 mg for pain reduction after gynecologic surgery compare with placebo
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Registration Number
TCTR20170809002
Lead Sponsor
none
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Female
Target Recruitment
36
Inclusion Criteria

1)body mass index below or equal 35 kg/m2
3)American Society of Anesthesiologists physical status (ASA) classification class I-II
4)Appointment to explore laparotomy for gynecologic surgery include total abdominal hysterectomy(TAH) with or without oophorectomy, salpingectomy, omentectomy, or lymphadenectomy
5)General anesthesia
6)Understand and can use visual analogue scale (VAS)
7)Understand and can use patient controlled analgesia (PCA)

Exclusion Criteria

1)Allery to gabapentin or opioid
2)underlying disease of epilepsy, psychiatric disease, or chronic pain
3)Use addictive substance or analgesic within 48 hours before surgery
4)Ovarian or fallopian tube cancer
5)Expect for long operation than 4 hours

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Post-operative pain score 2,4,8,12,24 hours after gynecologic surgery Visual analogue scale (VAS)
Secondary Outcome Measures
NameTimeMethod
Total morphine use(mg) 24 hours after operation 24 hours after operation Patient controlled analgesia (PCA) with morphine (mg),Side effect of morphine or gabapentin use(nausea,vomiting,dizziness,headache,fatigue,pruritis,etc) Within 24 hours after gynecologic surgery Observation and questionaire
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