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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00760253
Other study ID # 200807070R
Secondary ID
Status Completed
Phase N/A
First received September 25, 2008
Last updated December 14, 2009
Start date September 2008
Est. completion date December 2008

Study information

Verified date December 2008
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

This study is to find the fewer side effects formula of anesthesia for TVOR patients, to compare the BIS level during emergence and to find the correlation between BIS and transcutaneous carbon dioxide concentration.


Description:

Transvaginal oocyte retrieval (TVOR) is a procedure often used in infertility women . During the procedure, sedation, analgesia or anesthesia are often required. Propofol and alfentanyl are used for these patients for years, but these drugs are used in intravenous form and can be found in follicular fluid. Although further investigation needs to be undertaken to investigate any potential influence on fertilization and implantation rates, we anesthesiologist want to lower the use of drugs in these women. Target-controlled infusion (TCI) pumps can estimate and calculate the target and plasma concentration of propofol. By using these pumps , we can estimate the stable concentration of drugs. Besides, Bispectral index (BIS) monitor can help us to evaluate awareness or unarousable amnesia when we turn lower the drug use and keep patients amnesia during the procedure. Transcutaneous carbon dioxide monitor (tcCO2) can mimic the level of CO2 in patients by using noninvasive method. During anesthesia, CO2 will retain and may induce CO2 nacrosis, so we use these noninvasive method to help us to detect CO2 level preventing CO2 nacrosis and to see if there are any relationship with BIS.


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Study Design

Observational Model: Case Control, Time Perspective: Prospective


Locations

Country Name City State
Taiwan Department of Anesthesiology, National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

References & Publications (9)

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Outcome

Type Measure Description Time frame Safety issue
Primary Vital signs changes and side effects of drugs among groups pre-anesthesia, post-anesthesia, and one hour post-anesthesia No
Secondary Correlation between transcutaneous carbon dioxide and BIS (bispectral index) From drug infusion stopped to patients awake (per minute) No
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