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Clinical Trials/NCT00922142
NCT00922142
Completed
Not Applicable

Cesarean Postoperative Pain Satisfaction With Intravenous Patient-Controlled Analgesia Intravenous, Oral, or Epidural Method

Saint Elizabeth Regional Medical Center1 site in 1 country120 target enrollmentJune 2009
ConditionsCesarean

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cesarean
Sponsor
Saint Elizabeth Regional Medical Center
Enrollment
120
Locations
1
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

Hypothesis:

There is no significant difference in Cesarean patients' perceptions of overall pain management satisfaction between methods used for postoperative pain management.

Detailed Description

There is a significant difference between Cesarean patients' perceptions of advantages and disadvantages of three postoperative pain management methods identified by obstetrical patients. Participants will be introduced to study by anesthesia personnel in labor and delivery. The subject will be informed of the desire for their input on their perceived satisfaction with their chosen method for post-operative pain management and will be asked to participate in an anonymous survey by their second day after surgery. They will be informed that this is voluntary. Method of post-operative medication administration will be determined by attending physician to be either: epidural, IVPCA, or oral medication. Methods will be initiated in recovery room or the operative suite. Subjects will be identified on a postpartum admission log and a screening log will be created for study purposes. Informed Consents will be obtained. The screening log entries will be numbered corresponding to a numbered survey. The screening log will contain demographic and other patient identifiers including age, ethnicity, parity, presence of labor prior to cesarean, admission status of baby, cost associated with method and presence of rescue drugs and costs of rescue drugs and method services. Refusal information, exclusion criteria, and time/date of survey completion will also be recorded. This log will be maintained under lock and key.

Registry
clinicaltrials.gov
Start Date
June 2009
End Date
December 2009
Last Updated
14 years ago
Study Type
Observational
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • English speaking post-operative cesarean patients

Exclusion Criteria

  • Cesarean patients with know fetal demise
  • General/Local Anesthetic Method for Cesarean

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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