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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02166775
Other study ID # 5541
Secondary ID
Status Terminated
Phase N/A
First received June 14, 2014
Last updated April 4, 2016
Start date January 2014
Est. completion date March 2016

Study information

Verified date April 2016
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: ANSM- Agence Nationale de sécurité des Medicaments et produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

In this trial, the correlation between the psychopathological profile and sagittal balance unexplored to date spine will be studied. Indeed, a number of patients who benefited from well-conducted surgical treatment, targeted and tailored to their pathology, respond poorly to it. The investigators wonder if there are biomechanical factors or factors of psychopathological order which might influence the effectiveness of treatment. This seems logical for the entire medical community, but it has never been demonstrated in a clinical trial.


Description:

The purpose of this study is to find a global diagnostic and standardized tool , easy to use, on psychopathological factors influencing the posture of the patients lombalgia so that in this will be used to use identify upstream surgery, the patients undergoing psychiatric treatment of mood rather than surgical treatment. And thus may economise a surgical operation and its complications and the related expenses.


Recruitment information / eligibility

Status Terminated
Enrollment 205
Est. completion date March 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Men and women aged 18 to 70 years ·

- Spine surgery outpatients with or without low back pain with radicular ·- Affiliated to a social security scheme,

- Having signed an informed consent and were informed of the results of the consultation prior to inclusion

Exclusion Criteria:

- Patients having the major diseases of the spine: deformities (scoliosis, kyphosis), tumors, fractures, inflammatory and metabolic ·

- Patients having a spinal surgery history ·

- Patients difficult to inform ( emergency ward patients, patients with difficulties in oral comprehension)

Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Dr SCHULLER Sébastien Service de Chirurgie du Rachis, HUS Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary sagittal balance of the spine : - kyphosis in depressed or anxious patients- lordosis in patients with manic The primary endpoint was to compare the L1S1 lordosis measured in degrees relative to L1S1 lordosis expected, i-e the pelvic tilt +/- 10 ° and analyzed in relation to anxiety scores given by the Scale Hamilton Anxiety (HAM-A), depression with the Hamilton depression Scale (HAM-D) and hypomania using the Young Mania Rating Scale (YMRS). regarding the HAM-A, greater than or equal to 17 score will be considered as indicative of anxiety. For the HAM-D greater than or equal to 13 score will be considered indicative of depression. For the YMRS, greater than or equal to 20 score will be considered as indicative of a manic syndrome. It is obvious that the higher the score, the higher the importance of the disorder will be. 2 hours No
Secondary link between the psychopathological profile and questionnaires The secondary endpoints are finding a link between the psychopathological profile of patients using self-administered questionnaires. 2 hours No