Postoperative Pain After Implementation of Standardized Pain Therapy Management in Orthopaedic Patients (PAIN)

S

Schulthess Klinik

Status

Not yet enrolling

Conditions

Postoperative Pain, Acute

Treatments

Procedure: Standardized pain management

Study type

Observational

Funder types

Other

Identifiers

NCT06363227
ANEST-0003

Details and patient eligibility

About

The aim of this study is to examine the impact of implementing a standardized pain therapy protocol and their components on postoperative pain trajectories and postoperative outcomes such as increased opioid consumption and to compare it for different orthopaedic operations, i.e. major shoulder, hip, knee und spine surgery.

Full description

A multimodal standardized pain management was implemented at the Schulthess Clinic in 2002, followed by the gradual introduction of a standardized ultrasound-guided perioperative regional anaesthesia program. Along with these measures, an improved preoperative screening process for patients at risk of increased post-operative pain has been installed and an improved individual pain assessment in the perioperative period has been introduced. This allowed for the creation of pain trajectories, which the pain team started to use to identify gaps in the management of different patient groups. An example of a trajectory group is shown in Figure 1. These pain trajectories have not yet been evaluated for the overall implementation cycle of the multimodal standardized pain management in order to further improve postoperative care especially for patients with a history of chronic pain and those prone to opioid overconsumption.We hypothesise that pain trajectories have changed significantly over the study period as standardised pain management has been implemented. We also hypothesise that patients with chronic pain and increased opioid consumption will have different pain trajectories compared to all other patients. However, we believe that the pain trajectories for different orthopaedic surgeries do not show much variation.

Enrollment

12,000 estimated patients

Sex

All

Ages

16 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing primary hip and knee arthroplasties or revision surgery:CHOP Code: 81.51, 81.52, 81.52, 81.54
  • Patients undergoing primary shoulder or revision surgery: CHOP codes: 81.80.11, 81.80.12, 83.64.11, 81.82.35, 81.82.45, 81.82.46, 81.82.47
  • Patients undergoing major spine surgery: CHOP Code: 7A.6, 7A.7

Exclusion criteria

- Patients who did not sign general informed consent (for the Schulthess Clinic).

Trial contacts and locations

0

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Central trial contact

Christoph K Hofer, MD; Julia Item, PhD

Data sourced from clinicaltrials.gov

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