Analgesia After Cesarean Section

This study has been completed.
Sponsor:
Information provided by:
Seoul National University Bundang Hospital
ClinicalTrials.gov Identifier:
NCT01360060
First received: May 17, 2011
Last updated: May 24, 2011
Last verified: May 2011

May 17, 2011
May 24, 2011
December 2010
March 2011   (final data collection date for primary outcome measure)
Change of numeric rating scale (NRS) of postoperative pain during postoperative period [ Time Frame: postoperative 1, 2, 3, and 4 day ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01360060 on ClinicalTrials.gov Archive Site
  • incidence of stopping of intravenous PCA during postoperative 4 days [ Time Frame: during postoperative 4 days ] [ Designated as safety issue: No ]
  • serum magnesium level of group P [ Time Frame: preoperative 1 h and postoperative 1 day ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Analgesia After Cesarean Section
Not Provided

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.

Not Provided
Observational
Observational Model: Case Control
Time Perspective: Retrospective
Not Provided
Not Provided
Non-Probability Sample

medical record review

  • Preeclampsia
  • Pregnancy
Drug: Magnesium Sulphate
Magnesium sulphate was infused for the management of preeclampsia at perioperative period.
  • Group N
    parturients who had undergone Cesarean section under the diagnosis of non-preeclampsia
  • Group P
    parturients who had undergone Cesarean section under the diagnosis of preeclampsia
    Intervention: Drug: Magnesium Sulphate
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
503
March 2011
March 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • parturients undergoing Cesarean section
Female
20 Years to 50 Years
No
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
NCT01360060
Mg_section
Not Provided
Hyoseok, Na/professor, Seoul National University Bundang Hospital
Seoul National University Bundang Hospital
Not Provided
Not Provided
Seoul National University Bundang Hospital
May 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP