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The effect of oral glucose in pregnant women

Effect of oral glucose on bio-physical profile score in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012120111628N1
Enrollment
94
Registered
2013-01-19
Start date
2012-12-21
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

Pregnant women. Supervision of normal pregnancy

Interventions

Intervention 1: The case group will consume 50 g oral glucose dissolved in 200 cc of water. Intervention 2: The control group will consume 200 cc of water.
The case group will consume 50 g oral glucose dissolved in 200 cc of water.
The control group will consume 200 cc of water.

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women; gestational ages between 32 to 40 weeks; singleton pregnancy; fetus without anomalies and exclusion criteria: hypertension and diabetes mellitus.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Score bps include of Fetal breathing movements, fetal movements, fetal tone, fetal heart rate, speed, volume of amniotic fluid. Timepoint: Pre-intervention and post-intervention. Method of measurement: For each vaiable, if the patient has normal conditions then score of 2 is recorded. Otherwise, no score is recorded. The highest possible score for a natural birth rate of 10 and the lowest score is zero.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Behzad Tanghatari

Kermanshah University of Medical Sciences

btanghatari@kums.ac.ir+98 83 1727 2751

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 5, 2026