Evaluation of Different Anesthesia for Uterine Curettage
NCT ID: NCT00733564
Last Updated: 2009-03-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
150 participants
INTERVENTIONAL
2008-08-31
2009-03-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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1
Paracervical block will be performed
Lidocaine
Paracervical injection of 2% Lidocaine to block associated nociception input
2
Propofol anesthesia will be performed
Propofol
Propofol 3mg/kg will be injected intravenously; 1 mg/kg will be added additionally for incomplete anesthesia
3
Sevoflurane anesthesia will be performed
Sevoflurane
Sevoflurane 8% for anesthesia induction, 2-3% as the maintenance
Interventions
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Lidocaine
Paracervical injection of 2% Lidocaine to block associated nociception input
Propofol
Propofol 3mg/kg will be injected intravenously; 1 mg/kg will be added additionally for incomplete anesthesia
Sevoflurane
Sevoflurane 8% for anesthesia induction, 2-3% as the maintenance
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Performing abortion operation (medical- or surgical)
* Requiring painless abortion
Exclusion Criteria
* History of central active drugs administration
* Drug abuse
* Hypertension
* Diabetes
* Any other chronic diseases
* Allergy to the study drugs
* Habit of over-volume alcohol drinking
* Records of history of centrally active drug use and psychiatry
* Any organic disorder
19 Years
45 Years
FEMALE
No
Sponsors
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Nanjing Medical University
OTHER
Responsible Party
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Nanjing Medical University
Principal Investigators
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XiaoFeng Shen, MD
Role: STUDY_DIRECTOR
Nanjing Medical University
Locations
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Nanjing Maternal and Child Health Care Hospital
Nanjing, Jiangsu, China
Countries
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Other Identifiers
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NJFY0890-MZ12
Identifier Type: -
Identifier Source: secondary_id
NMU-FY2008-209
Identifier Type: -
Identifier Source: org_study_id