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CompletedNCT00922142Updated Jul 20, 2011

Cesarean Postoperative Pain Satisfaction

An observational study in Cesarean, sponsored by Saint Elizabeth Regional Medical Center. Completed at 1 site in United States. Open to female participants aged 14 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-07-20.

Sponsored by Saint Elizabeth Regional Medical Center · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
120
Ages
14 Years to 40 Years
Sex
Female
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Study summary

Hypothesis:

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

Read the 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.

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Conditions studied

  • Cesarean

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03

In context

Pain, Postoperative

5,089 studies on the registry are indexed under Pain, Postoperative; 1,137 are open to participants now.

This study's enrollment of 120 is above the median of 102 across 607 observational studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Saint Elizabeth Regional Medical Center is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

post-operative cesarean patients

Inclusion criteria

  • English speaking post-operative cesarean patients

Exclusion criteria

Exclusion Criteria:

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

Observational model
Case-control
Time perspective
Prospective
Enrollment
120 participants (actual)
Biospecimen retention
Samples without dna
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Study locations

1 site
  • Saint Elizabeth Regional Medical Center
    Lincoln, Nebraska 68510, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 20, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00922142
Lead sponsor
Saint Elizabeth Regional Medical Center
First posted
Jun 17, 2009
Start date
Jun 2009
Primary completion
Aug 2009
Completion
Dec 2009
Last update
Jul 20, 2011

Study contacts

Deb Chambers, RN
principal investigator · Saint Elizabeth Regional Medical Center

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2011. You cannot join it, but the record below documents what was studied.

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