A clinical trial to study the effectiveness of ââ?¬Å?Generalization of Rubricsââ?¬? in treating Typhoid fever
- Conditions
- Health Condition 1: 3- AdministrationHealth Condition 2: A010- Typhoid fever
- Registration Number
- CTRI/2022/09/045665
- Lead Sponsor
- DR M SATISH KRISHNA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Individuals between ages 12 to 60 years of age comprising both genders
Diagnosed Cases of Typhoid fever with clinical symptoms and Rapid dot EIA test or widal positive results
Temperatures between 99F to 104F
Participants with informed consent
Participants who are mentally sound and who can express their sufferings
Patients with severe Dehydration
Those febrile patients who had received antibiotic treatment for their symptom within 4 days prior to coming to the hospital OPD
Those who were diagnosed for other known febrile illness like malaria haemorragic fevers fevers of viral etiology etc
Known cases of Typhoid fever where the subject has a history of cardiac disorders peptic or gastric ulcerations convulsions and any other major complications
Pregnant women Children with underlying malnutrition and those infected with multidrug resistant isolates
Known cases with history of other bleeding disorders
Diagnosed cases of Typhoid fever with inflammation of pericardium myocardium or to pancreas
Participants who are deaf and dumb or those who cannot express or narrate the symptoms feelings or sufferings
Withdrawal criteria
If improvement is not present within 7 days case shall be referred
Cases going into complications like uncontrolled abdominal pain abdominal guarding not responding to treatment intestinal perforation shall be referred
Non responding cases of delirium.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Typhoid fever is completely reduced - Even in conditions where relevant rubrics are absent to the symptoms elicitedTimepoint: 14days
- Secondary Outcome Measures
Name Time Method General feeling of well beingTimepoint: 14days