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Efficacy and Safety of Ivermectin and Doxycycline in Combination or IVE Alone in Patients With COVID-19 Infection.

Phase 2
Completed
Conditions
COVID-19 Patients
Interventions
Registration Number
NCT04407130
Lead Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Brief Summary

Burden:

Initial outbreak of corona virus disease 2019 (COVID-19) was reported from Wuhan, China in early December 2019.Presently known to be caused by a novel beta-corona virus, named as Severe acute respiratory syndrome corona virus 2 ( SARS-CoV-2).

World Health Organization (WHO) declared a pandemic on March.

The clinical characteristics of COVID-19 include respiratory symptoms, fever, cough, dyspnoea and pneumonia

Infected individuals exhibit:

1. Mostly mild illness (80% +) recover without any treatment (\~80%)

2. Moderate illness that needs hospitalization and recovers after standard

3. supportive treatment (\~14%)

4. Critical illness (\~5%) needs ICU support

5. Death (1-2% )

COVID-19 has now spread \>210 countries and territories globally. SARS-CoV-2 is a respiratory virus which spreads primarily through droplets generalized when an infected person coughs or sneezes or through droplets of saliva or discharge from the nose.

Symptomatic management remains the mainstay of treatment strategy. Mortality appears to be more common in older individuals and those with co-morbidities, such as chronic lung disease, cardiovascular disease and diabetes. Young people with no comorbidities also appear to be at risk for critical illness including multi-organ failure and death. Seen more in Bangladesh between 21-40 yrs of age.

Knowledge Gap:

There is no specific treatment against this new virus that WHO has officially declared until now.There are many pharmacologic therapies that are being used or considered for treatment of COVID-19. National Guidelines on Clinical Management of Corona virus Disease 2019 (Covid-19): V 5.0 date 9th April 2020) CDC, DGHS, GoB

Thus an RCT is urgently needed in Bangladesh: Based on recent literatures on Rx studies in COVID-19 patients from other countries as well as its availability \& affordability of those repurposed medicines

Detailed Description

Objectives:

General Objective:

The aim of the study is to evaluate efficacy and safety of ivermectin in combination with doxycycline or ivermectin alone for the treatment of hospitalized SARS-CoV-2 infected adult Bangladeshi COVID-19 +ve patients and to compare with placebo; where all three arms will receive the standard care of treatment of COVID-19 infected patients in the hospital. By successful demonstration of the safety and efficacy of these repurposed medicines, it may have the potential to play an important role in the treatment of COVID-19+ve patients.

Specific Objective:

1. Duration of the virological clearance rate

2. Days required for remission of fever and cough

Secondary Objective:

* Patients requiring oxygen

* Patients failing to maintain SpO2 \>88 despite oxygenation

* Number of days on oxygen support

* Chest X-ray improvement

* Duration of hospitalization

* All cause mortality

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria

Not provided

Exclusion Criteria
  • Allergy to ivermectin or doxycycline; or other contraindications to any of the study medications
  • History of chronic heart disease (IHD, heart failure, documented cardiomyopathy etc)
  • History of chronic liver disease (SGPT value more than 3 times of normal value)
  • History of chronic kidney disease (S. Creatinine for male >1.3 mg/dL or >115 µmol/L and for female >1.2 mg/dL or >106.1 µmol/L)
  • Pregnant or lactating women
  • Participated in any other clinical trial within last 4 weeks
  • H/o received Ivermectin/Doxycycline within last 7 days

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Tab IvermectinIvermectin + PlaceboIvermectin - 200 mcg/kg (12 mg tablet) once per day D1-D5 + Placebo two tablets D1 followed by Placebo one tablet D2-5
PlaceboPlaceboDrug: Placebo 3 Placebo tablets D1 followed by 2 tablets D2-5
Tab Ivermectin +Cap DoxycyclineIvermectin + Doxycycline + Placebo200 mcg/kg (12 mg tablet) ivermectin (IVERA) single dose and 200 mg stat doxycycline day-1 followed by 100mg doxycycline 12hrly for 4 day (i.e. day2-day5) + Placebo one tablet D2-5
Primary Outcome Measures
NameTimeMethod
Remission of coughwithin 7 days after enrollment

• Remission of cough: No signs of cough showing respiratory rate within 12-20/ min, on day7

Remission of feverwithin 7 days after enrollment

• Body temperature will be \< 37.5 C by day 7 detected by Infrared thermometer

Virological clearancewithin 7 days after enrollment

• Presence of virus will be negative on Day 7 detected by RT PCR

Secondary Outcome Measures
NameTimeMethod
Patients requiring oxygenwithin 7 days after enrollment

Detected SPO2 level \<94% on Day 7or before by pulse oxymeter

Patients failing to maintain SpO2 >93% despite oxygenationwithin 7 days after enrollment

Patients who fail to maintain pulse oxymeter detected SpO2 level\>93% despite O2 supplementation of 2-6 L/min, on Day 7 or before

Number of days on oxygen supportwithin 7 days after enrollment

Any number of days on oxygen support on Day 7 or before recorded in CRF

Duration of hospitalizationwithin 14 days after enrollment

Hospital stay ≥7days to ≤14 days as per CRF records

All causes of mortalitywithin 14 days after enrollment

Death any time during 14 days of study period from any cause recorded in CRF and Hospital death certificate

Trial Locations

Locations (1)

Icddr,B

🇧🇩

Dhaka, Bangladesh

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