Comparison of the blood values of interleukin 6 of pregnant ladies undergoing vaginal and cesarean delivery

comparison of serum interleukin-6 of parturients undergoing vaginal and caesarean delivery - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/08/071894

Enrollment

Registered

2024-08-05

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: O- Medical and Surgical Health Condition 2: O298- Other complications of anesthesiaduring pregnancy Health Condition 3: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: Group cesarean section: blood samples will be collected from patients undergoing cesarean section within10 minutes of delivery Intervention2: Group cesarean section: Blood samples will

Eligibility

Inclusion criteria

Inclusion criteria: This prospective will be conducted on parturients who undergo normal delivery or elective caesarean section.

Exclusion criteria

Exclusion criteria: Parturients with multiple pregnancies, history of chorioamnionitis, fever, premature rupture of membrane, use of corticosteroid or use of medications that affect the immune system will be excluded

Design outcomes

Primary

Measure	Time frame
To compare IL6 between normal delivery and cesarean sectionTimepoint: immediately following delivery of baby	—

Secondary

Measure	Time frame
to compare postpartum rise in maternal temperature more than 38 degree celsiusTimepoint: till discharge	—

Countries

India

Contacts

Public ContactDr Aswathi C

Amrita Institute of medical Sciences

aswathicnambiar@gmail.com09495962020

Outcome results

None listed

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