Carolinas Medical Center, Department of Orthopaedic Surgery
Charlotte, North Carolina, 28204, United States
NCT Number: NCT02701192
The purpose of the study is to analyze the outcomes of patients with coccygodynia (pain in and around the coccyx region) treated with coccygectomy (a procedure during which the coccyx is removed) and to report on the rate of complications of the procedure. The study will also aim to find pre-operative clinical predictors of good outcomes after coccygectomy. The investigators hypothesize that coccygectomy will not improve scores on the Short Form-36 (SF-36), Oswestry Disability Scale (ODI), tolerable sitting time, or Visual Analog Pain Scale (VAS). Also, the investigators hypothesize that there are no independent variables associated with improved outcomes.
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Notify Me18 year and older
All sexes
Observational
Charlotte, North Carolina, 28204, United States
Coccygodynia can be a functionally limiting and painful disease with conservative treatment providing mixed results. When proper surgical indications are met, results seem to be promising. However, there is a lack of data in the literature to support surgical treatment. The case series reports currently in the literature are small and retrospective with ill-defined selection criteria. To date there has been no study prospectively following patients undergoing coccygectomy. This type of study could accurately obtain data prospectively. This information will help better guide the clinician through treatment of this disease.
All patients will be seen and enrolled through an outpatient spine specialty clinic of the senior author. Patients that meet the inclusion criteria will be offered enrollment in the study by a third party (clinical research assistant). Patients enrolled will then complete pre-treatment SF-36, Oswestry Disability Scale and a pain visual analog scale. Patients will be followed at 2 weeks, 6 weeks, 3 months, 6 months, 1 year and 2 years after treatment. Patients will complete the questionnaire containing the VAS and tolerable sitting time at all visits with SF-36 and Oswestry disability scale completed at one year post treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patient receiving coccygectomy surgery.
Time frame: Baseline,1 year and 2 years
Patients will complete the100mm Visual Analog Scale (VAS) at Baseline and 2 years after procedure. Patient will be instructed to indicate pain intensity by marking a 100mm line where one end, 0 indicates no pain and 100 indicates extreme pain on the other end.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
The SF-36 is on a 0-100 scale, with higher scores indicating a more favorable/better health state.
Time frame: Baseline,1 year and 2 years
Oswestry Disability Index used to measure a patient's permanent functional disability. Scores range from 0 to 100. scores between 0 and 20 described as "minimal disability", scores between 21and 40 described as "moderate disability",scores between 41and 60 described as "severe disability",scores between 61 and 80 described as "crippled" and scores between 81 and 100 described as " bed bounded"
Time frame: Baseline,1 year and 2 years
Complication rates after coccygectomy surgery
Time frame: Baseline,1 year and 2 years
Threshold for treatment success was based on a minimum clinically importance difference (MCID) of 20 points on the oswestry disability index at 2 year follow-up and an overall oswestry disability index score of <22 points.
Wake Forest University Health Sciences
Other
Acronym: Coccyx
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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