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Comparison of early and immediate oral hydration on post-cesarean section outcome

Comparison of early and immediate oral hydration on post-cesarean section outcome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220517054893N1
Enrollment
26
Registered
2022-05-25
Start date
2022-07-02
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Hospital stay length. Onset (spontaneous) of labor after 37 completed weeks of gestation but before 39 completed weeks gestation, with delivery by (planned) cesarean section

Interventions

Intervention 1: Intervention group: In the intervention group, oral fluid therapy for patients will begin during the first two hours after surgery. Intervention 2: Control group: In the control group,

Sponsors

Zanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women undergoing cesarean section by spinal anesthesia

Exclusion criteria

Exclusion criteria: Hypertention Body mass index more than 30 Preeclampsia Heart disease

Design outcomes

Primary

MeasureTime frame
Hospital stay length. Timepoint: Days of hospitalization after surgery. Method of measurement: Based on day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAida Rezaei

Zanjan University of Medical Sciences

aida.rezaei@zums.ac.ir+98 21 8806 4148

Outcome results

None listed

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