Status:
COMPLETED
Comparison of Analgesic Efficacy of Fentanyl, Sufentanil and Butorphanol After Remifentanil Anesthesia
Lead Sponsor:
Nanjing Medical University
Conditions:
Postoperative Pain
Eligibility:
FEMALE
19-45 years
Phase:
PHASE4
Brief Summary
Fast awakening from anesthesia is one of the major characteristics of remifentanil-associated anesthetic induction and maintenance, whereas corresponding pain during awakening influences patient's reh...
Eligibility Criteria
Inclusion
- ASA physical status I-II
- Chinese
- 19-45yr
- Selective laparoscopic surgeries
Exclusion
- Allergy to opioids, a history of the use of centrally-acting drugs of any sort, chronic pain and psychiatric diseases records
- Participants younger than 18 years, older than 45 years or pregnancy was eliminated
- Due to the significant changes in vital signs might affect cognition of pain and that of sensation, over 20% variation of these records from the baselines or below 92% of SpO2 under 20-40% nasal tube oxygen at any time should be excluded from the study
- Those who were not willing to or could not finish the whole study at any time
Key Trial Info
Start Date :
July 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2009
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT00738192
Start Date
July 1 2008
End Date
March 1 2009
Last Update
March 11 2009
Active Locations (1)
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1
Nanjing Maternal and Child Health Care Hospital
Nanjing, Jiangsu, China, 210004