Evaluate the Efficacy and Safety of Andrographolide Sulfonate in Patients With Acute Tonsillitis
- Conditions
- Acute Tonsillitis
- Interventions
- Registration Number
- NCT03134443
- Lead Sponsor
- Jiangxi Qingfeng Pharmaceutical Co. Ltd.
- Brief Summary
A multicenter, randomized, single-blind, placebo-controlled,phase 4 clinical trial to evaluate the efficacy and safety of andrographolide sulfonate in patients with acute tonsillitis
- Detailed Description
The patient after passing the screening, with the ratio of 1:1, were randomly assigned to experimental group and control group. Experimental group: On the basis of conventional therapy,combined with xiyanping injection(andrographolide sulfonate) 10-20ml/d, with 0.9% normal saline 100ml-250ml diluted intravenous drip (not with other drugs in the same container mixed use), control drip speed per minute of 30-40 drops. control group: Xiyanping injection simulation(0.9% normal saline) 10-20ml/d,the treatment method is the same as the experimental group. Treatment cycle: less than 7 days (the longest period of treatment is 7 days, if the clinical symptoms were relieved in the treatment, patients were stoped treatment).
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 144
- 1.18-65 years, males or females;
- 2.patients met the acute tonsillitis diagnosis;
- 3.patients'all symptoms (including cough) appeared no longer than 72 h before inclusion to the trial
- 4.patients compliance is good, written informed consent was obtained from all participants before the study.
- 1.Patients had a history of andrographolide sulfonate or andrographolide allergy.
- 2.Pregnancy, lactation, and absence of contraception in women of fertile age.
- 3.Judging by the researchers, Past or present illness of patients may affect to participate in the trial or affect the outcome of the study, including cardio-pulmonary diseases, malignant diseases, autoimmune diseases, hepatorenal disease, blood diseases, nervous system diseases, immune system diseases and endocrine diseases.
- 4.After checking, Patients with pulmonary tuberculosis, bronchial asthma, bronchial pneumonia, bronchiectasis, pneumoconiosis, silicosis, lung cancer, pulmonary infiltration or other allergic respiratory diseases and other chronic lung diseases
- 5.Patients using systemic steroids or other immunosuppressive therapy
- 6.Patients with severe cardiopulmonary dysfunction, abnormal liver and kidney function, blood system diseases.
- 7.Patients are alcohol (daily drink alcoholic wine is more than 40g) or drug abuse or drug addicts in the past year.
- 8.Patients were participated in any study of drug trials in the last 30 days.
- 9.According to the researchers' judgment, anyone who are not suitable for the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description control group Andrographolide sulfonate simulation Xiyanping injection simulation(andrographolide sulfonate simulation) 10-20ml/d, The treatment method is the same as the experimental group. Experimental group Andrographolide sulfonate Xiyanping injection(andrographolide sulfonate) 10-20ml/d, with 0.9% normal saline 100ml-250ml diluted intravenous drip (not with other drugs in the same container mixed use), control drip speed per minute of 30-40 drops.
- Primary Outcome Measures
Name Time Method cured rate less than 7 days clinical symptoms and signs totally disappear, the period of lab tests return to normal is recorded
- Secondary Outcome Measures
Name Time Method effective time window less than 7 days days range from treatment is received to the effectiveness is observed, and symptoms disappear
time from admission to recovery of sore throat less than 7 days the time of sore throat relief and purulent secretions complete disappearance of in the tonsils
time from admission to recovery of fever less than 7 days In the absence of other antipyretic drugs, the time from Xiyangping injection beganning to use to Axillary temperature below 37.5℃ , and last more than 24 hours without fever.
the incidence of complications less than 7 days Such as, the incidence of Acute otitis media, acute rhinitis, acute bronchitis, acute bronchitis,and so on.
bacterial eradication rate less than 7 days bacterial eradication rate=Sputum culture negative cases after treatment /sputum culture positive cases before treatment x 100%
days of antibiotic use less than 7 days oral anti infective Drugs use days and intravenous Anti infective Drugs use days are recorded
number of participants with treatment-related adverse events less than 7 days the total incidence of adverse events,the incidence of adverse events associated with Xiyanping injection, the incidence of patients with grade 3 through grade 4 adverse events that are related to study drug, graded according to NCI-CTC V4.0 .
Observe and record all adverse events and serious adverse events, including physical examination, vital signs, laboratory tests (Hematology, blood biochemistry, urine routine, stool routine), ECG changes and so on.
Trial Locations
- Locations (1)
The First Affiliated Hospital of Nanchang University
🇨🇳Nanchang, Jiangxi, China