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The Effect of Syringe Type on Adverse Effect Following Immunization.

The Effect of Syringe Type on Adverse Effect Following DTP Vaccine Immunization, a Randomized Clinical Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201107317171N1
Enrollment
1000
Registered
2011-10-09
Start date
2012-01-15
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: sever local reaction following immunization. Condition 2: sever local reaction following immunization. Infection following immunization Other complications following immunization, not elsewhere classified

Interventions

Intervention 1: DTP vaccine is administrated by type B syringe. Intervention 2: DTP vaccine is administrated by type A syringe.
DTP vaccine is administrated by type B syringe
DTP vaccine is administrated by type A syringe

Sponsors

Shahroud University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 6 Years

Inclusion criteria

Inclusion criteria: All children who are eligible for DTP vaccination can be registered in this study. every eligible child is not enrolled in study If DTP vaccination is contraindicated, his/her parents denied to sign informed consent or the child is not accessible for follow up of AEFI (adverse effects following immunization ).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Erythema. Timepoint: days 2, 4 and 6 following immunization. Method of measurement: By health care professional and/or physician.;Oedema. Timepoint: days 2, 4 and 6 following immunization. Method of measurement: By health care professional and/or physician.;Pain. Timepoint: days 2, 4 and 6 following immunization. Method of measurement: By health care professional and/or physician.;Fever. Timepoint: days 2, 4 and 6 following immunization. Method of measurement: By health care professional and/or physician.

Secondary

MeasureTime frame
Sever local reaction AND Injection-Site Abscess. Timepoint: Days 2, 4, and 6 after immunization. Method of measurement: By health care professional and/or physician.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMansooreh Fateh, MD, MPH

Shahroud university of Medical Sciences

fateh@shmu.ac.ir; fateh45908@yahoo.com+98 27 3222 0062

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026