Overview

Improving Pain Management and Long Term Outcomes Following High Energy Orthopedic Trauma (Pain Study)

Status:
Completed
Trial end date:
2018-12-31
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to definitively resolve questions regarding the use of multimodal pharmacologic pain management for orthopedic trauma patients in the context of a multicenter, randomized clinical trial. Also, as a significant proportion of this population develops chronic post traumatic osteoarthritis (PTOA), a sub-objective of this study is to examine the etiology and incidence of chronic pain and PTOA in this population.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Major Extremity Trauma Research Consortium
Treatments:
Ketorolac
Ketorolac Tromethamine
Meloxicam
Polystyrene sulfonic acid
Pregabalin
Criteria
Inclusion Criteria:

1. Patients with one of the following types of injuries:

1. Unilateral, Grade I &II open or closed pilon (distal tibial plafond), calcaneus,
talus fractures and Lisfranc dislocations requiring operative treatment with
fixation; or

2. Unilateral, open (type I, II, or IIIA) ankle fractures with associated
dislocation on presentation (OTA 44B3 or 44C) requiring operative treatment with
fixation; or

3. Unilateral, open or closed distal and proximal humerus (OTA 11A-C and OTA 13
A-C); or

4. Open femoral shaft fracture (OTA 32 A-C; Gustilo Type I-IIIC) or open or closed
supracondylar femur fractures (OTA 33 A-C); or

5. Open or closed tibial plateau or shaft fractures (OTA 42 A-C or 43 A-C)

6. Any combination of the above injuries which are surgically treated as a whole

2. Patients who present to the admitting hospital acutely or clinic following an initial
assessment in the Emergency Department, for care up to 10 days following initial
injury.

3. Patients 18-80 years old inclusive.

4. Patients who are English or Spanish competent.

5. Treating physicians agree that none of the study drugs are indicated for standard of
care treatment for this patient.

6. Patients able to be followed at the METRC facility for at least 12 months following
injury.

Exclusion Criteria:

1. Patients unable to provide informed consent.

2. Patients with chronic pain being presently treated with opioid or gabapentinoid
prescription or any other alternative therapy.

3. Patients who are current IVDA

4. Patients with bilateral or ipsilateral injuries requiring surgery

5. Patients with other orthopedic or non-orthopedic injuries requiring operative
intervention

6. Patients with severe osteopenia.

7. Patients who are skeletally immature (defined as less than 18 years of age or no
radiographic evidence of epiphyseal closure).

8. Patients who are expected to have a post-surgical stay less than 24 hours.

9. Patients with a history of allergy to any drugs in the study.

10. Patients unable to swallow oral medications or without adequately functioning GI
tract.

11. Patients with a history of gastrointestinal bleeds or gastric perforation.

12. Patients with a history of stroke or heart attack.

13. Patients currently receiving an aspirin or NSAID regimen (exception: low dose (81 mg)
aspirin. See section 6.5) Patients with any bleeding disorders.

14. Patients with severe renal failure. Patients with moderate renal failure may
participate in the study at a modified dose. See Section 9.6.

15. Patients undergoing daily treatment with systemic glucocorticoids before surgery.

16. Patients using angiotensin-converting enzyme (ACE) inhibitors, who may be at increased
risk of developing angioedema with pregabalin.

17. Patients likely to have severe problems maintaining follow-up, including patients
diagnosed with a severe psychiatric conditions, patients who live too far outside the
hospital's catchment area, patients who are incarcerated and patients who have
unstable housing situations.

18. Patients who experienced a loss of consciousness consistent with a clinical diagnosis
of a closed head injury, or concern of a cerebrovascular bleed secondary to traumatic
brain injury.

19. Patients with a GCS <15

20. Patient speaks neither English nor Spanish.

21. Patients who are pregnant or lactating at time of screening