Effectiveness of a Bivalent Killed Whole Cell Based Oral Cholera Vaccine
NCT01508507 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 240
Last updated 2013-06-05
Summary
Various field studies has found that the modified , bivalent, whole cell - based oral cholera vaccine (OCV) to be safe, immunogenic and effective with protective efficacy of 67 % in earlier clinical trials. However, the effectiveness of the vaccine in "real" life situation using the public health system is unknown. It is critical to follow up in the same population, where pilot introduction of OCV was introduced and evaluate vaccine proactive effectiveness at individual as well as at population level. The follow - up and determination of effectiveness of mass OCV vaccination was requested by State Government.
Conditions
- Cholera
Sponsors & Collaborators
-
Department of Health and Family Welfare, Orissa
collaborator OTHER -
Regional Medical Research Center, Orissa
collaborator UNKNOWN -
International Vaccine Institute
lead OTHER
Principal Investigators
-
Shantanu K Kar, MD · Director, Regional Medical Research Center, Bhubanewar, Orissa, India
-
Thomas F Wierzba, PHD · International Vaccine Institute
Eligibility
- Min Age
- 1 Year
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-03-31
- Primary Completion
- 2014-02-28
- Completion
- 2014-03-31
Countries
- India
More Related Trials
-
Safety and Immunogenicity of Locally Manufactured New (HL-OCV) Oral Cholera Vaccine
NCT02823899 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Safety and Immunogenicity of a Killed Oral Cholera Vaccine in Infants
NCT00548054 ·Status: UNKNOWN ·Phase: PHASE2
-
Immunogenicity of One Versus Two Doses of Killed Oral Cholera Vaccine
NCT00419133 ·Status: COMPLETED ·Phase: PHASE2
-
A Post-marketing Observational Study of Oral Cholera Vaccine
NCT07300462 ·Status: NOT_YET_RECRUITING ·Phase: PHASE4
-
Follow-up of Pregnant Women After a Mass Vaccination of Oral Cholera Vaccine (ShancholTM) in Nsanje Malawi
NCT02499172 ·Status: TERMINATED ·Phase: NA
-
A Study of Two Doses of Oral Cholera Vaccine (Shanchol™) in Subjects Aged 1 Year and Older in the Philippines
NCT01949675 ·Status: COMPLETED ·Phase: PHASE4
-
Immune Non-Inferiority, Safety and Lot-to-Lot Consistency of Oral Cholera Vaccine-Simplified Compared to Shanchol™
NCT04760236 ·Status: COMPLETED ·Phase: PHASE3
-
A Phase III Randomized, Modified Double-blind, Multi-centric, Comparative Study, to Evaluate the Non-inferiority of Immunogenicity and Safety of Hillchol® (BBV131)to Shanchol™ Along With Lot-to-lot Consistency of Hillchol®(BBV131).
NCT05507229 ·Status: UNKNOWN ·Phase: PHASE3
-
VAXCHORA Pediatric Study to Assess Safety and Immunogenicity
NCT03220737 ·Status: COMPLETED ·Phase: PHASE4
-
To Evaluate Safety of Oral Cholera Vaccine Hillchol® (BBV131)
NCT05732766 ·Status: UNKNOWN ·Phase: PHASE3
-
A Study of Two Doses of Oral Cholera Vaccine (Shanchol™) in Subjects Aged 1 Year and Older in Dominican Republic
NCT02434822 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Safety of Tetravalent Rotavirus Vaccine in Healthy Indian Adult Male Volunteers
NCT01091298 ·Status: COMPLETED ·Phase: PHASE1
-
Phase 1b Ascending Dose Study of PanChol in Healthy Volunteers
NCT07107516 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1
-
Immunogenicity of Co-administered Oral Polio Vaccine and Oral Cholera Vaccine
NCT03581734 ·Status: UNKNOWN ·Phase: PHASE3
-
Evaluation of Recombinant Norovirus Hexavalent Vaccine in Healthy Subjects
NCT05805618 ·Status: NOT_YET_RECRUITING ·Phase: EARLY_PHASE1
-
The Oral Hexavalent Reassortant Rotavirus Attenuated Live Vaccine (Vero Cells)
NCT06950645 ·Status: COMPLETED ·Phase: PHASE1
-
Long-term Immunogenicity and Safety of Fourth Administration of Boryung Cell-Culture Japanese Encephalitis Vaccineinj
NCT02532569 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Immunogenicity Study of the Tetravalent Rotavirus Vaccine
NCT01061658 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Immunologic Responses to a Live Attenuated Oral Cholera Vaccine
NCT03251495 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase III Clinical Trial to Evaluate the Protective Efficacy of Three Doses of Oral Rotavirus Vaccine (ORV) 116E
NCT01305109 ·Status: UNKNOWN ·Phase: PHASE3
-
Diarrhea and Bivalent Oral Polio Vaccine Immunity
NCT01559636 ·Status: COMPLETED ·Phase: NA
-
CDC-9 Inactivated Rotavirus Vaccine (IRV) Intramuscular (IM) Phase 1 Clinical Trial in Healthy Adults
NCT06485258 ·Status: COMPLETED ·Phase: PHASE1
-
Phase I Clinical Trial of Inactivated Rotavirus Vaccine in a Population Aged 6 Weeks-49 Years Old
NCT06350058 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
PhaseⅡClinical Trial of Oral Hexavalent Reassortant Rotavirus Attenuated Live Vaccine (Vero Cells)
NCT06967272 ·Status: RECRUITING ·Phase: PHASE2
-
Healthy Adult Volunteer Study for Two Doses of a Shigella Vaccine
NCT00210288 ·Status: COMPLETED ·Phase: PHASE2