CTRI/2020/12/029575
Not yet recruiting
Phase 3
A study to assess the safety and efficacy of add-on Unani regimen in preventing the progression of severity of the disease in mild to moderate symptomatic COVID-19 RT-PCR positive cases
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: B972- Coronavirus as the cause of diseases classified elsewhereHealth Condition 2: J09- Influenza due to certain identified influenza viruses
- Sponsor
- Central Council for Research in Unani Medicine
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. On the day of admission patients who have been tested positive with SARS\-CoV2 virus through RT PCR
- •2\. Patients with mild symptoms
- •Patients with moderate symptoms with respiratory rate \< 30 per minute and oxygen saturation \> 90%
Exclusion Criteria
- •1\.COVID\-19 patients with symptoms classified as severe or critical.
- •2\.Suspected COVID\-19, not tested positive for COVID\-19 by RT\-PCR
- •3\.Persons with severe primary respiratory disease or pneumonia
- •4\.Pregnant and lactating women
- •5\.Persons with severe illness such as Cancer, Heart Disease, Stroke, Mental disorder, etc., and who are considered to be excluded from the study as evaluated by the Investigators
- •6\.COVID\-19 positive cases simultaneously participating as subjects in the interventional arm of other COVID\-19 clinical trials
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Investigation of efficacy and safety of add-on therapy with DPP-4 inhibitor in type 2 diabetic patients poorly controlled with basal supported oral therapyType 2 diabetesJPRN-UMIN000010849Department of Metabolism & Endocrinology Juntendo University Graduate School of Medicine40
Recruiting
Phase 2
Evaluation of the efficacy and safety of lacosamide to duloxetine in the treatment of taxanes- induced peripheral neuropathyTaxane-induced neuropathy.IRCT20090613002027N21Mazandaran University of Medical Sciences60
Completed
Phase 2
Olanzapine as a medication to reduce nausea and vomiting following chemotherapy in childrePalliative care.Encounter for palliative careIRCT20090613002027N14Sari University of Medical Sciences49
Active, not recruiting
Not Applicable
A trial, in which subjects with type 2 diabetes, who qualify for treatment intensification, are given insulin degludec and, additionally, either liraglutide or insulin aspart, both in combination with metformin, with the largest meal. The purpose is to compare efficacy and safety of these two treatments.EUCTR2011-001493-25-ATovo Nordisk A/S420
Active, not recruiting
Not Applicable
A trial, in which subjects with type 2 diabetes, who qualify for treatment intensification, are given insulin degludec and, additionally, either liraglutide or insulin aspart, both in combination with metformin, with the largest meal. The purpose is to compare efficacy and safety of these two treatments.Type 2 diabetesMedDRA version: 14.0Level: LLTClassification code 10045242Term: Type II diabetes mellitusSystem Organ Class: 10027433 - Metabolism and nutrition disordersTherapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18]EUCTR2011-001493-25-DEovo Nordisk A/S420