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NCT01360060 Clinical Trial

Analgesia After Cesarean Section

Pregnancy Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01360060
Other study ID # Mg_section
Secondary ID
Status Completed
Phase N/A
First received May 17, 2011
Last updated May 24, 2011
Start date December 2010
Est. completion date March 2011

Study information
Verified date May 2011
Source Seoul National University Bundang Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

Magnesium sulphate is the first line therapy for the management of preeclampsia and eclampsia in obstetrics. Perioperative administration of magnesium sulphate has been proved to be an effective as an analgesic adjuvant. The investigators evaluated the analgesic effect of magnesium in parturients undergoing Cesarean section.

Recruitment information / eligibility
Status Completed
Enrollment 503
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- parturients undergoing Cesarean section

Study Design

Observational Model: Case Control, Time Perspective: Retrospective

Related Conditions & MeSH terms

Intervention

Drug:
• Magnesium Sulphate
Magnesium sulphate was infused for the management of preeclampsia at perioperative period.

Locations
Country Name City State
Korea, Republic of Seoul national university bundang hospital Seongnam Gyeonggi

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Bundang Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change of numeric rating scale (NRS) of postoperative pain during postoperative period postoperative 1, 2, 3, and 4 day No
Secondary incidence of stopping of intravenous PCA during postoperative 4 days during postoperative 4 days No
Secondary serum magnesium level of group P preoperative 1 h and postoperative 1 day No
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