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The effect of increased intravenous hydration on the course and out come of labor in nulliparous women during 1387.

the effect of increased intravenous hydration on duration of labor and type of delivery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201105256575N2
Enrollment
120
Registered
2011-07-16
Start date
2008-09-22
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

Increased Intravenous Hydration of Nulliparous in Labor. Single spontaneous delivery

Interventions

Intervention 1: The second, groupreceived 60 ml of lactated Ringer’s solution IV per hour. Intervention 2: The first group (usual care) received lactated Ringer’s solution IV per hour whenever they ne
Treatment - Drugs
The second, groupreceived 60 ml of lactated Ringer’s solution IV per hour
The first group (usual care) received lactated Ringer’s solution IV per hour whenever they needed based on obstetrical condition.
The third group received 120 ml of lactated Ringer’s solution IV per hour
The fourth groupreceived 240 ml of lactated Ringer’s solution IV per hour

Sponsors

Vice chancellor for research, Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:Iranian nationality;35-18 years of age ;primiparous, singleton pregnancy;gestational age38-40;without CPD; optimal care during pregnancy;blood pressure less than 140/90 mmHg; body mass index 19/8-26(kg m) before pregnancy;beginning of the active phase of labor with cervical dilatation 4 cm ; intact of membran ;estimated fetal weight less than 4000 grams; Excluding criteria : Polyhydramnios;abnormal presentation;preeclampsia;pyelonephritis ;any other febrile illnesses in the last 48 hours;known medical conditions before and during pregnancy such as asthma; cardiovascular disease;diabetes;kidney disease or cratinin more than 1 at the admission time; disorders of gastroenteritis during the last 48 hours; symptoms of dehydration in the last 48 hours

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of labor. Timepoint: start of active phase to 24h after delivery. Method of measurement: duration of labora ccording to minute.

Secondary

MeasureTime frame
Type of delivery. Timepoint: type of delivery. Method of measurement: type of delivery vaginal or cesarean.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAshraf Direkvand-Moghadam

Department of Midwifery,Faculty of Nursing and Midwifery,Ilam University of Medical Sciences

direkvand-a@medilam.ac.ir+98 918 342 0061

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 26, 2026