Assessment of intravenous sedation effect on pain of surgical removing polyps compared with local anesthesia
Not Applicable
- Conditions
- polypectomy.Polyp of corpus uteri
- Registration Number
- IRCT2016031426855N3
- Lead Sponsor
- Tehran University of Medical Sciences , Deputy of Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 84
Inclusion Criteria
patients aged between 18- 50 years old with polyps less than 3 cm; no history of cardiopulmonary diseases.
Exclusion criteria: Lidocaine sensitivity; excess anxiety.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The pain of surgery. Timepoint: During and 3 hours after surgery ( in general anesthetic group: only the pain of 3 hours after surgery). Method of measurement: Visual analogue scale.
- Secondary Outcome Measures
Name Time Method Post operative recurrence of polyp. Timepoint: 6 months after surgery. Method of measurement: Ultrasound.;Duration of operation. Timepoint: From anesthesia induction to discharge of recovery room. Method of measurement: Hour.;Complications of analgesia method. Timepoint: During analgesia, during surgery and 3 hours after surgery. Method of measurement: Check list.