Clinical Trials Directory

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UnknownNCT03134443

Evaluate the Efficacy and Safety of Andrographolide Sulfonate in Patients With Acute Tonsillitis

Combined With Andrographolide Sulfonate on the Basis of Conventional Therapy in the Treatment of Acute Tonsillitis: a Randomized, Single Blind, Placebo-controlled, Multicenter Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
144 (estimated)
Sponsor
Jiangxi Qingfeng Pharmaceutical Co. Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGAndrographolide sulfonateRoutine treatment for acute tonsillitis + Xiyanping injection
DRUGAndrographolide sulfonate simulationRoutine treatment for acute tonsillitis + Xiyanping injection simulation

Timeline

Start date
2016-12-01
Primary completion
2017-12-31
Completion
2018-06-01
First posted
2017-05-01
Last updated
2017-05-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03134443. Inclusion in this directory is not an endorsement.