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Bupivacaine local infiltration at trocar insertion sites after gynecologic laparoscopic surgery: A randomized, double-blind, placebo-controlled clinical trial

Phase 4
Conditions
Bupivacaine local infiltration at trocar insertion sites after gynecologic laparoscopic surgery control pain decrease pain score than saline
Gynecologic Laparoscopic Surgery, postoperative pain, bupivacaine
Registration Number
TCTR20210904001
Lead Sponsor
Obstetrics gynecologic department
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Enrolling by invitation
Sex
Female
Target Recruitment
80
Inclusion Criteria

1. Female who has gynecologic laparoscopic surgery with 4-port entry
2. Can listening and reading Thai language
3. Thai nationality
4. No history of bupivacaine allergy or local anesthetic. Allergy
5. No psychiatric disorder
6. No history of medication for control pain in 1 week before
7. Accepted to volunteer in this research project

Exclusion Criteria

1. Female who has gynecologic laparoscopic surgery with port entry less than 4 ports site
2. Who have change laparoscopic surgery convert to laparotomy
3. Volunteers who can leave from journal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pain At 2,4,8,12,24 hours after intervention Record pain score 0-10 In postoperative at 2,4,8,12,24 hours after surgery ( abdominal pariatal pain, abdominal visceral pain, left shoulder pain , right shoulder pain
Secondary Outcome Measures
NameTimeMethod
umber of opioid use 72 hour after surgery Number of patient who have opioid use and amount of opioid in patients use ,Adverse effect of bupivacaine 72 hours af surgery Such as : skin rash, seizure, Nausea, Headache, Dizziness, Slow heart rate, Blurred vision ,hearing loss
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