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Postoperative Pain Management in Hospital and Following Discharge From Hospital.

Assessment of Postoperative Pain Management in Patients Undergoing Total Knee Arthroplasty Immediately After Surgery and Following Discharge From Hospital.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01907178
Enrollment
200
Registered
2013-07-24
Start date
2014-07-31
Completion date
2015-06-16
Last updated
2017-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthropathy of Knee Joint

Keywords

total knee arthroplasty

Brief summary

To investigate postoperative pain management in patients undergoing knee or hip replacement while they are in the hospital and following discharge to their home. Additionally, sample questions will be asked prior to surgery to predict patient's postoperative pain experience.

Detailed description

We hypothesize that patients experience more postoperative pain at home than they do in hospital and factors such as preoperative anxiety, depression, and preoperative pain affect the level of postoperative pain experienced by patients. A total of 200 patients undergoing total knee surgery will be enrolled in this observational study. They will be asked to fill a baseline questionnaire including demographic information, medical problems, anxiety, depression, preoperative pain level, etc. Following routine standard anesthesia and surgery, patient's pain will be assessed every 4 hours when they are in the hospital after surgery, then daily assessment for 1 week after they are discharged home followed at 2 months, and 6 months after surgery.

Interventions

None listed

Sponsors

Trinity Health Of New England
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing total knee arthroplasty

Exclusion criteria

* Patients attending rehabilitation facilities after discharge * unwilling or unable to provide consent

Design outcomes

Primary

MeasureTime frameDescription
Pain scoresduring hospital stay (average 3 days)Pain scores (at rest & with exercise) will be collected during the hospital stay

Secondary

MeasureTime frameDescription
preoperative anxiety scorespreoperativeAnalysis of preoperative anxiety scores.
Preoperative depression scorespreoperativeAnalysis of preoperative depression score.

Other

MeasureTime frameDescription
Pain medication consumptionduring hospital stay (average 3 days)pain medication consumption will be collected during hospital stay

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026