Simple Bone Cysts in Kids (SBoCK)
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ClinicalTrials.gov Identifier: NCT02193841 |
Recruitment Status :
Recruiting
First Posted : July 18, 2014
Last Update Posted : March 8, 2023
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Condition or disease | Intervention/treatment | Phase |
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Bone Cyst | Procedure: Curettage with puncture (C & P) Device: Curette Device: Vitoss morsels | Phase 3 |
In general, few randomized clinical trials have been undertaken in paediatric orthopaedics, and only one to date has addressed the problem of simple bone cysts (SBCs). Also known as unicameral bone cysts, they are the commonest bone lesion in children. Despite general opinion, these cysts do not resolve at skeletal maturity.
Many forms of treatment have been recommended but none, including the popular methods of corticosteroid or bone marrow injections, have reliably eradicated SBC. Although the lesions are considered benign (non-cancerous), they cause pain, frequently interfere with function, dramatically restrict play activity, may re-fracture leading to growth arrest and/or deformity, and cause enormous anxiety for children and their families.
With a well-developed network of surgeons and researchers, we will provide evidence comparing the effectiveness of two treatment interventions for SBC. More specifically, our goals for this study are:
- to compare the rate of radiographic healing between two standard treatments including curettage with puncture alone, and curettage with puncture followed by injection with Vitoss morsels;
- to identify prognostic radiographic factors associated with simple bone cyst healing and fracture;
- to determine the impact of simple bone cyst on children/family functioning.
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 160 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double (Participant, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Simple Bone Cysts in Kids (SBoCK) |
Study Start Date : | March 2015 |
Estimated Primary Completion Date : | March 2027 |
Estimated Study Completion Date : | March 2027 |
Arm | Intervention/treatment |
---|---|
Active Comparator: C & P
Curettage with puncture (C & P) will be performed alone
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Procedure: Curettage with puncture (C & P)
A curette will be inserted to scrape the contents of the cyst (curettage) and a hole in the cyst wall will be made (puncture) near the bone marrow cavity Device: Curette A small surgical instrument with a rounded edge designed for scraping |
Active Comparator: C & P with Vitoss
A predetermined amount of Vitoss morsels will be injected following the curettage and puncture (C & P)
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Procedure: Curettage with puncture (C & P)
A curette will be inserted to scrape the contents of the cyst (curettage) and a hole in the cyst wall will be made (puncture) near the bone marrow cavity Device: Curette A small surgical instrument with a rounded edge designed for scraping Device: Vitoss morsels A bone substitute intended for use as a filler for voids or gaps in bones
Other Name: Tri-calcium phosphate bone graft substitute |
- Cyst healing [ Time Frame: 2 years ]Healing will be graded according to a 4-point modified Neer's classification by radiologists
- Clinical measures (Cyst features) [ Time Frame: 1 and 2 years ]Cyst features (ie. appearance, size) will be described or measured from X-rays taken annually after treatment
- Functional measures (Questionnaire scores) [ Time Frame: 1 and 2 years ]Function in participants will be evaluated using self-reported questionnaires for activity level, perception of illness, and pain annually after treatment

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Ages Eligible for Study: | 2 Years to 21 Years (Child, Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Patients with a confirmed simple bone cyst in a long bone (ie. arm or leg) within last 3 months
- At least 3 weeks must have elapsed since last fracture
- At least 3 months must have elapsed since last cyst treatment
- Patients and/or their legal representatives willing to provide written informed consent (and assent, when appropriate)
- Patients with stabilizing implants in the bone where the cyst is located
Exclusion Criteria:
- Patients with bone disease (ie. osteogenesis imperfecta, cancer, osteoporosis, Paget's disease)
- Pregnant or breastfeeding female
- Patients with cysts crossing the growth plate (area where bone grows)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02193841
Contact: Julie Shiu | julie.shiu@sickkids.ca |

Principal Investigator: | James G. Wright | The Hospital for Sick Children | |
Principal Investigator: | Sevan Hopyan | The Hospital for Sick Children |
Publications:
Responsible Party: | James Wright, Orthopaedic Surgeon, The Hospital for Sick Children |
ClinicalTrials.gov Identifier: | NCT02193841 |
Other Study ID Numbers: |
1000042364 |
First Posted: | July 18, 2014 Key Record Dates |
Last Update Posted: | March 8, 2023 |
Last Verified: | March 2023 |
Simple bone cyst Unicameral bone cyst |
Cysts Bone Cysts Neoplasms Pathological Conditions, Anatomical Bone Diseases |
Musculoskeletal Diseases Calcium Calcium-Regulating Hormones and Agents Physiological Effects of Drugs |