Title

Investigations of Mechanisms and Treatment in Post-traumatic Joint Contractures
Randomized, Double Blind, Placebo Controlled Trial of Ketotifen in Patients With Elbow Fractures or Dislocations
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Intervention/Treatment

    ketotifen ...
  • Study Participants

    152
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:

any problems with the study medication
any new conditions or concerns that have developed

The participant was reminded:

of next visit
to continue to take study drug as instructed

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.
Study Started
Jun 30
2013
Primary Completion
Aug 31
2017
Study Completion
Aug 31
2017
Last Update
Mar 27
2018

Drug Ketotifen

5 mg PO bid

  • Other names: Zaditen

Drug Placebo

5 mg placebo PO bid

  • Other names: Lactose Placebo

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.

Criteria

Inclusion Criteria:

Age ≥ 18 years old
Isolated distal 1/3 humerus fractures
Proximal 1/3 ulna fractures
Proximal 1/3 radial fractures
Elbow dislocations
Open fractures with or without nerve injury
Presentation to Peter Lougheed Centre (PLC), Foothills Medical Centre (FMC) or South Health Campus (SHC).

Exclusion Criteria:

Pre-existing elbow contracture
Osteoarthritis of affected elbow
Inflammatory arthritis of affected elbow
Gout of affected elbow
Nonspecific monoarticular arthritis of the affected elbow
Inability to give informed consent due to irreversible cognitive disorder
Inability to comply with post-operative physiotherapy
Injury > 7 days at the time of presentation
Inability to mobilize elbow injury within 2 weeks of injury or surgery
Pregnancy
Breast feeding
Oral hypoglycemic medications
History of epilepsy
Lactose intolerance
No Results Posted