ITMCTR2000004102
Not Yet Recruiting
Phase 4
A prospective non-randomized controlled clinical study evaluating the effectiveness and safety of Yuye Jiedu Granules in the treatment of children with influenza wind-heat and dampness syndrome
The First Teaching Hospital of Tianjin University of TCM0 sitesTBD
ConditionsChildhood influenza
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Childhood influenza
- Sponsor
- The First Teaching Hospital of Tianjin University of TCM
- Status
- Not Yet Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •(1\) Meet the clinical diagnostic criteria for influenza in children, and the rapid influenza antigen test (colloidal gold immunochromatographic method) is positive;
- •(2\) Meet the TCM syndrome differentiation standard of wind\-heat and dampness;
- •(3\) Aged from 1 to 13 years old (\<14 years old);
- •(4\) Course of fever \<\=48h;
- •(5\) The informed consent process complies with the regulations, and the legal representative or the child (\>\=8 years old) jointly signs the informed consent form.
Exclusion Criteria
- •(1\) Suffering from pharyngeal conjunctival fever, herpetic angina, purulent tonsillitis, etc.;
- •(2\) Influenza complications such as sinusitis, otitis media, bronchitis, pneumonia, nervous system damage, heart damage, myositis and rhabdomyolysis, septic shock have occurred;
- •(3\) Severe or critical cases of influenza;
- •(4\) Antiviral drugs have been used within 48 hours before this visit;
- •(5\) Have received influenza vaccine within 12 months before the start of the test;
- •(6\) Receiving steroid therapy or other immunosuppressive therapy systemically;
- •(7\) History of epilepsy or high fever convulsion;
- •(8\) Patients with severe malnutrition, rickets, and serious primary diseases of the heart, brain, liver, kidney and hematopoietic system;
- •(9\) Allergic to test drugs;
- •(10\) According to the judgment of the investigator, there are other diseases or conditions that reduce the possibility of enrollment or complicate enrollment, such as unstable living environment, inconvenient transportation, etc. that may easily cause loss to follow\-up.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not Yet Recruiting
N/A
A Clinical Study for the Effect of Shenbing Prescription on Gastrointestinal Function after Gynecological Abdominal SurgeryGynecological patients after abdominal surgeryITMCTR1900002272Guangdong Provincial Hospital of Chinese Mediciine
Not Yet Recruiting
Phase 1
A prospective, randomized and controlled clinical study on the treatment of diabetes nephropathy with chronic kidney disease (stage 3-4) by Chen's Tangshen recipeITMCTR2200006505onghua Hospital Shanghai University of Traditional Chinese Medicine
Recruiting
Phase 1
A prospective, randomized and controlled clinical study of traditional Chinese medicine (Astragalus / Panax notoginseng) combined with a new oncolytic virus / fusion cell vaccine in the treatment of advanced liver cancer and lung cancerung cancer, liver cancer\Various malignant tumorsITMCTR2000003215The First Affiliated Hospital of Guangxi University of traditional Chinese Medicine
Recruiting
N/A
MantraTM Surgical Robotic System, Model 3.0 - Interventional Clinical Study for 10 patients.CTRI/2024/06/068556Sudhir Srivastava Innovations Pvt. Ltd
Completed
N/A
Comparing Two Different Regional Anaesthetic Techniques With Standard IV Analgesic Technique For Post-Operative Pain Management In Patients Undergoing Laproscopic Cholecystectomy.Health Condition 1: O- Medical and SurgicalCTRI/2023/03/050416ABHINAV NANDA111