The analgesic efficacy of nefopam after gynecologic laparoscopy surgery
Not Applicable
- Conditions
- Diseases of The genitoruinary system
- Registration Number
- KCT0004212
- Lead Sponsor
- Chungnam National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- 135
Inclusion Criteria
? Patients between 20 and 70 years of age who underwent laparoscopic gynecologic surgery through general anesthesia
? American Society of Anesthesiologists (ASA) physical status classification I,II
? Weight 40 ~ 75kg
? Patients who signed the agreement
Exclusion Criteria
? patient's refusal
? Fentanyl or nefopam hypersensitive or allergic
? If the patient is undergoing analgesic treatment before surgery
? If the patient is pregnant or is pregnant
? myoma or tumor surgery
? Unregulated medical illness
: Gastrointestinal ulcers, heart failure, uncontrolled diabetes, severe infection.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS scores up to 48 hours postoperatively
- Secondary Outcome Measures
Name Time Method PCA usage time and usage;Assess whether PCA is disabled;Patient bolus frequency;The frequency and severity of nausea and vomiting;Patient satisfaction