ITMCTR2000003788Not yet recruitingPhase 1
Clinical Study on Treatment of Postoperative Syndrome of Lumbar Spine with the Method of Nourishing Qi, Nourishing Blood and Nourishing Liver and Kidney
Conditions
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional study
Eligibility Criteria
- Ages
- 18 to 80 (—)
- Sex
- All
Inclusion Criteria
- •1. The age is generally 18-80 years old;
- •2. Meet the diagnostic criteria of postoperative lumbar syndrome;
- •3. Understand the purpose of the study and be willing to follow the randomized treatment plan;
Exclusion Criteria
- •1. Cerebrospinal fluid leakage in the operation area after lumbar spine surgery or a second operation on the lumbar spine
- •2. Have a history of lumbar spine tumor, lumbar spine tuberculosis, lumbar spine trauma, lumbar spine infection, ankylosing spondylitis or lumbar spine deformity;
- •3. Have a history of coagulopathy, lupus erythematosus, diabetic neuropathy, rheumatoid arthritis or other serious medical diseases;
- •4. Pregnant women, people with psychotropic drug dependence or cognitive impairment.
Investigators
Similar Trials
Active, not recruiting
Not Applicable
Observational Study of Postoperative Treatment in the Cases of Complete Excision for Non-Small-Cell Lung Cancer of Pathological Stage I (T1>2 cm, TNM Classification Version 6)Advanced lung cancerJPRN-UMIN000015732C-03 Executive committee5,000
Recruiting
Phase 1
Clinical study on the prevention of postoperative recurrence and metastasis of colorectal cancer by Zuojin pill combined with adjuvant chemotherapycolorectal cancerITMCTR2000003349Shuguang Hospital affillated with Shanghai University of TCM
Not yet recruiting
Not Applicable
Retrospective study of postoperative management of robot-assisted rectal resection performed at our hospitalJPRN-UMIN000035017Department of anesthesiolgy, Sapporo medical university school of medicine40
Active, not recruiting
Not Applicable
Klinische Studie zum Einfluss einer postoperativen Verabreichung von (S)-(+)-Ketamin auf das Schmerzempfinden nach großen chirurgischen Eingriffen - Ketanest®S-Schmerz-StudiePostoperatives Schmerzempfinden bei elektiven großen bauchchirurgischen Eingriffen, transabdominellen urologischen Eingriffe oder transabdominellen gynäkologischen EingriffenEUCTR2006-000714-20-ATDr. Wolfgang Jaksch150
Recruiting
Phase 4
Clinical study on improving postoperative symptoms of cervical spondylotic myelopathy by Qishe pillCervical spondylotic myelopathyITMCTR1900002834onghua Hospital Shanghai University of Traditional Chinese Medicine
