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The Optimal Duration of Preoperative Anti-tuberculosis Treatment of Spinal Tuberculosis

The Study of Standardized Preoperative Anti-tuberculosis Treatment of Surgical Treatment of Spinal Tuberculosis Patients

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02477852
Enrollment
400
Registered
2015-06-23
Start date
2015-04-30
Completion date
2017-12-31
Last updated
2015-06-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tuberculosis, Spinal

Keywords

tuberculosis, spinal, general, operation, drug, therapy

Brief summary

The purpose of this study is to determine the better preoperative anti-tuberculosis treatment period of patients with spinal tuberculosis.

Detailed description

Quality assurance plan:All the investigators will receive uniform training. Standard cases follow-up,collection,management systems will be established.The process of cases follow-up,collection,management will be supervised by the third party.Data entry will be in the manner of independent parallel entry.The endpoints events are judged by third party.Statistical analysis are implemented by the statistics institutions of the third party.In order to control the bias,this study takes multicenter,random,control study design. Sample size assessment:Under the condition of multicenter,random,control design, computational formula takes the rate comparisons of two groups.The key endpoints event is soft tissue width of vertebral side measured by computed tomography. The incidence of the key endpoints event in two weeks group is 30%.The incidence of the key endpoints event in four weeks group is 15%.When alpha value is 0.5 and power value is 0.9,the sample size is 161 patients.If loses visit rate is 20%,the sample size is 194 patients. Statistical analysis plan:The key events are analyzed by chi-squared test.The statistical significance factors among them are calculated by relative risk. Data checks and source data verification are supervised by a third-party organization (contract research organization,CRO). Standard Operating Procedures:Investigator's brochure has explained in detail about the standard operating procedures of everything.Data dictionary can be found in standard operating procedures. Plan for missing data: The investigators Set a 20% rate of lost to follow-up.

Interventions

DRUGIsoniazid

preoperative treatment of spinal tuberculosis with Isoniazid

DRUGRifampicin

preoperative treatment of spinal tuberculosis with Rifampicin

DRUGEthambutol

preoperative treatment of spinal tuberculosis with Ethambutol

DRUGPyrazinamide

preoperative treatment of spinal tuberculosis with Pyrazinamide

Sponsors

Beijing Municipal Science & Technology Commission
CollaboratorOTHER
Beijing Chest Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients are diagnosed as spinal tuberculosis clinically,and they do not receive antituberculosis therapy or with 2 weeks. * The age is between 15 years old and 75 years old. * Patients have good compliance,and have clear surgical indications.4.Willing to join the research

Exclusion criteria

* Patients have surgical contraindications. * Patients have bad habits:taking drug,drinking.3.Patients have mental disease. * Patients have bad compliance. * Patients have hematogenous disseminated pulmonary tuberculosis, serious central nervous system tuberculosis,and serious extrapulmonary tuberculosis. * Patients with drug resistance for Antituberculosis drugs,and patient have to change the treat plan,and patients have immunodeficiency diseases. * Patients are not diagnosed as spinal tuberculosis clearly. * Not willing to join the research

Design outcomes

Primary

MeasureTime frame
Vertebral side width of soft tissue is measured by CT after operation.up to 3 months

Secondary

MeasureTime frame
Amount of bone trabecula between bone graft surfaces is measured by X-ray after operation.up to 6 months

Countries

China

Contacts

Primary Contactshibing qin, doctor
ly13785361227@163.com86+10+13581557856
Backup Contactshi bi qin, doctor

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026