NCT00922142

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2009

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2009

Completed
15 days until next milestone

First Submitted

Initial submission to the registry

June 16, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 17, 2009

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2009

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2009

Completed
Last Updated

July 20, 2011

Status Verified

July 1, 2011

Enrollment Period

2 months

First QC Date

June 16, 2009

Last Update Submit

July 19, 2011

Conditions

Cesarean

Eligibility Criteria

Age14 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

post-operative cesarean patients

You may qualify if:

  • English speaking post-operative cesarean patients

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Saint Elizabeth Regional Medical Center

Lincoln, Nebraska, 68510, United States

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

no biospecimens to be retained

Study Officials

  • Deb Chambers, RN

    Saint Elizabeth Regional Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 16, 2009

First Posted

June 17, 2009

Study Start

June 1, 2009

Primary Completion

August 1, 2009

Study Completion

December 1, 2009

Last Updated

July 20, 2011

Record last verified: 2011-07

Locations

US(1)