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Optimization and evaluation of integrative traditional Chinese and western medicine therapy for cervical spondylosis based on combination of disease and syndrome

Optimization and evaluation of integrative traditional chinese and western medicine therapy for cervical spondylosis based on combination of disease and syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013222
Enrollment
Unknown
Registered
2017-11-02
Start date
2017-12-01
Completion date
Unknown
Last updated
2017-11-06

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

Conditions

cervical spondylosis

Interventions

treatment group:Pi zheng particles
control group I:Jin Kang Fu particle
control group II:Placebo of Pi zheng particles

Sponsors

Long Hua Hospital Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) patients who met the diagnostic criteria and TCM syndrome criteria; (2) patients who voluntarily accepted the treatment in this study; (3) Aged between 18~65 years old; (4) signed informed consent.;Inclusion criteria: (1) patients who met the diagnostic criteria and TCM syndrome criteria; (2) patients who voluntarily accepted the treatment in this study; (3) Aged between 18~65 years old; (4) signed informed consent.;Inclusion criteria: (1) patients who met the diagnostic criteria and TCM syndrome criteria; (2) patients who voluntarily accepted the treatment in this study; (3) Aged between 18~65 years old; (4) signed informed consent.;Inclusion criteria: (1) patients who met the diagnostic criteria and TCM syndrome criteria; (2) patients who voluntarily accepted the treatment in this study; (3) Aged between 18~65 years old; (4) signed informed consent.;Inclusion criteria: (1) patients who met the diagnostic criteria and TCM syndrome criteria; (2) patients who voluntarily accepted the treatment in this study; (3) Aged between 18~65 years old; (4) signed informed consent.

Exclusion criteria

Exclusion criteria: 1. refuse treatment and randomized grouping; 2. combined with cardiovascular disease, mental illness, suspected alcohol and drug abuse; 3. with image evidence of bone fracture or other bone disease; 4. intensive pain, with spinal cord compression and surgical indications; 5. receiving other treatment,witch may affect the observation of indexes for therapeutic effects in this study; 6. have skin diseases and infectious diseases; 7. allergic to "Methycobal" and "Jingfukang Granule "or the drug ingredients; 8. female patients who are pregnant; 9. cannot take treatment in other reasons.;Exclusion criteria: 1. refuse treatment and randomized grouping; 2. combined with cardiovascular disease, mental illness, suspected alcohol and drug abuse; 3. with image evidence of bone fracture or other bone disease; 4. intensive pain, with spinal cord compression and surgical indications; 5. receiving other treatment,witch may affect the observation of indexes for therapeutic effects in this study; 6. have skin diseases and infectious diseases; 7. allergic to "Methycobal" and "Jingfukang Granule "or the drug ingredients; 8. female patients who are pregnant; 9. cannot take treatment in other reasons.;Exclusion criteria: 1. refuse treatment and randomized grouping; 2. combined with cardiovascular disease, mental illness, suspected alcohol and drug abuse; 3. with image evidence of bone fracture or other bone disease; 4. intensive pain, with spinal cord compression and surgical indications; 5. receiving other treatment,witch may affect the observation of indexes for therapeutic effects in this study; 6. have skin diseases and infectious diseases; 7. allergic to "Methycobal" and "Jingfukang Granule "or the drug ingredients; 8. female patients who are pregnant; 9. cannot take treatment in other reasons.;Exclusion criteria: 1. refuse treatment and randomized grouping; 2. combined with cardiovascular disease, mental illness, suspected alcohol and drug abuse; 3. with image evidence of bone fracture or other bone disease; 4. intensive pain, with spinal cord compression and surgical indications; 5. receiving other treatment,witch may affect the observation of indexes for therapeutic effects in this study; 6. have skin diseases and infectious diseases; 7. allergic to "Methycobal" and "Jingfukang Granule "or the drug ingredients; 8. female patients who are pregnant; 9. cannot take treatment in other reasons.;Exclusion criteria: 1. refuse treatment and randomized grouping; 2. combined with cardiovascular disease, mental illness, suspected alcohol and drug abuse; 3. with image evidence of bone fracture or other bone disease; 4. intensive pain, with spinal cord compression and surgical indications; 5. receiving other treatment,witch may affect the observation of indexes for therapeutic effects in this study; 6. have skin diseases and infectious diseases; 7. allergic to "Methycobal" and "Jingfukang Granule "or the drug ingredients; 8. female patients who are pregnant; 9. cannot take treatment in other reasons.

Design outcomes

Primary

MeasureTime frame
VAS;DHI;JOA score;

Countries

China

Contacts

Public ContactWen Mo;Wen Mo;Wen Mo;Wen Mo;Wen Mo ;;;;

Long Hua Hospital Shanghai University of Traditional Chinese Medicine;Long Hua Hospital Shanghai University of Traditional Chinese Medicine;Long Hua Hospital Shanghai University of Traditional Chinese Medicine;Long Hua Hospital Shanghai University of Traditional Chinese Medicine;Long Hua Hospital Shanghai University of Traditional Chinese Medicine

mw2218@126.com;mw2218@126.com;mw2218@126.com;mw2218@126.com;mw2218@126.com+86 13801968271;+86 13801968271;+86 13801968271;+86 13801968271;+86 13801968271

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026