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| ID | Type | Description | Link |
|---|---|---|---|
| REB15-0081 | Other Identifier | Conjoint Health Research Ethics Board |
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| Name | Class |
|---|---|
| Canadian Institutes of Health Research (CIHR) | OTHER_GOV |
| American Society for Surgery of the Hand | OTHER |
| Workers' Compensation Board, Alberta | OTHER |
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Injured joints, especially at the elbow, are at risk for permanent motion loss, also known as joint contractures. Joint contractures limit the function of an elbow and are a recognized complication that occurs often after a traumatic injury. The benefits of early motion after injury has helped in preventing joint contractures but there are still several patients that develop debilitating joint contractures. Current research suggests that mast cells, which are found in the joint, are key in causing joint contractures. Research has been done using a medication called Ketotifen. Ketotifen has been linked to stabilizing mast cells and preventing the joint contracture. It is hoped that short-term use of this medication after an injury will prevent the contracture from occurring.
Individuals ≥ 18 years old with isolated distal 1/3 humerus and/or proximal 1/3 ulna and/or proximal 1/3 radius fractures and/or elbow dislocations (open fractures with or without nerve injury may be included) and presented to Peter Lougheed Centre (PLC), Foothills Medical Center (FMC), or South Health Campus (SHC).
Participants were required to take Ketotifen 5mg by mouth twice a day for 6 weeks or placebo twice a day by mouth for 6 weeks. Neither the participant nor the physician knew if the participant was taking Ketotifen or placebo. Sometimes this type of injury requires surgery. This study invited both patients that do and do not require surgery to participate.
We took a sample of blood to measure tryptase (normally found in the body). We predicted people with high levels of tryptase were more likely to develop stiffening in the joint.
Participants were asked to return for follow up visits 2, 6, 12, 24, and 52 weeks after surgery or date of initial injury if surgery was not required. These visits were part of normal care for this type of injury.
At the visit participants were asked to do the following, some of which was not part of normal care.
At each visit: Range of motion of the elbow was assessed, DASH score was completed- form helping the research group understand the level of disability from this injury, X-rays until the fracture was considered healed (this was normal treatment), SF12 - questionnaire about how the patient was feeling and coping with their injury, Additional information was collected about how the injury was healing and weight was measured.
The participant was required to have physiotherapy which is normal treatment for this injury.
The participant was contacted by telephone at week 1, 3, 4 and 5 while taking the study medication. During these times:
The participant was asked about:
The participant was reminded:
During these telephone contacts, if any problems were detected that could not be rectified or figured out during the telephone interview, then participant was asked to attend the Cast Clinic to see their doctor in person.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Operative, Ketotifen | Experimental | Ketotifen 5mg orally twice per day for 6 weeks. |
|
| Non-operative, Ketotifen | Experimental | Ketotifen 5mg orally twice per day for 6 weeks. |
|
| Operative, Placebo | Placebo Comparator | Placebo oral medication twice daily for 6 weeks. |
|
| Non-operative, Placebo | Placebo Comparator | Placebo oral medication twice daily for 6 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ketotifen | Drug | 5 mg PO bid |
|
| Measure | Description | Time Frame |
|---|---|---|
| Joint range of motion | Extension-flexion arc of motion | 12 months post-injury |
| Measure | Description | Time Frame |
|---|---|---|
| Range of motion | 2,6,12,24 and 52 weeks post injury | |
| Patients requiring (re)operation for elbow-related causes | 12 months | |
| Radiographic evaluation for fracture healing/non-union |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Kevin Hildebrand, MD | University of Calgary | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Peter Lougheed Centre | Calgary | Alberta | T1Y 6J4 | Canada | ||
| Foothills Medical Centre |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 32112583 | Background | Liu CS, Ademola A, Zhang M, Garven A, Kopka M, Salo PT, Hart DA, Befus AD, Hildebrand KA. Human serum mast cell tryptase levels in elbow fractures or dislocations and its association with injury severity. J Orthop Res. 2020 Sep;38(9):2015-2019. doi: 10.1002/jor.24642. Epub 2020 Mar 11. | |
| 32639394 | Derived |
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| ID | Term |
|---|---|
| D003286 | Contracture |
| D050723 | Fractures, Bone |
| D004204 | Joint Dislocations |
| ID | Term |
|---|---|
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D009135 | Muscular Diseases |
| D014947 | Wounds and Injuries |
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| ID | Term |
|---|---|
| D007665 | Ketotifen |
| ID | Term |
|---|---|
| D013876 | Thiophenes |
| D013457 | Sulfur Compounds |
| D009930 | Organic Chemicals |
| D010880 | Piperidines |
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| Placebo | Drug | 5 mg placebo PO bid |
|
|
| 12-52 weeks |
| Calgary |
| Alberta |
| T2N 1N4 |
| Canada |
| South Health Campus | Calgary | Alberta | Canada |
| Hildebrand KA, Schneider PS, Mohtadi NGH, Ademola A, White NJ, Garven A, Walker REA, Sajobi TT; PERK 1 Investigators. PrEvention of Posttraumatic contractuRes with Ketotifen 1 (PERK 1): A Randomized Clinical Trial. J Orthop Trauma. 2020 Dec 1;34(12):e442-e448. doi: 10.1097/BOT.0000000000001878. |
| D006573 |
| Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |