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Halogen light stimulation in fetal well being assessment

Effect of halogen light and vibroacoustic stimulation on nonreactive fetal heart rate pattern

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201011275261N1
Enrollment
100
Registered
2011-09-03
Start date
2010-04-21
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

Condition 1: fetal well being assessment. Condition 2: fetal well being assessment. Condition 3: fetal well being assessment. Condition 4: fetal well being assessment. Condition 5: fetal well being assessment. Fetus and newborn affected by maternal conditions that may be unrelated to present pregnancy Other conditions originating in the perinatal period Fetus and newborn affected by maternal complications of pregnancy Fetus and newborn affected by complications of placenta, cord and membrane

Interventions

Intervention 1: In halogen light stimulation, the halogen light source )CE Spotlight, YUYAO SHUNYE ELECTRICAL APPLIANCES CO.,LTD, China) luminance of 1000,000 candle power. The 10-cm diameter light
Diagnosis
In halogen light stimulation, the halogen light source )CE Spotlight, YUYAO SHUNYE ELECTRICAL APPLIANCES CO.,LTD, China) luminance of 1000,000 candle power. The 10-cm diameter light surface was pla
In vibroacoustic stimulation group an standard fetal stimulatory (FS-1 Fetal Stimulator, Edan Instruments, Inc. China) frequency of 80 Hertz for 3 seconds, above the symphysis was applied.If an adequ

Sponsors

Vice chancellory for research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: talking and undrestanding in Farsi; gestational age of 32-42; single and cephalic pregnancy; absence of known fetal abnormalities; no labour pain and vaginal bleeding. Exclusion criteria: any deceleration during nonstress testing.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Nonstress test results. Timepoint: the duration of testing time in reactive result , and in nonreactive pattern , the time is up to 20 minutes. Method of measurement: fetal heart rate record tracing in beats /minutes.;Time to acceleration. Timepoint: the time elapsed to begining of fetal heart rate reactivity. Method of measurement: fetal heart rate record tracing, beats/minutes.;Time to reactive pattern. Timepoint: the time elapsed to achive a reactive pattern (minutes). Method of measurement: fetal heart rate record tracing, beats/minutes.

Secondary

MeasureTime frame
Biophysical profile. Timepoint: after stimulated testing, regardless of esults, biophysical profile scoring was done for all ones up to 30 minutes. Method of measurement: sonography evaluation of four health qualities each one score of 2 and whole 8 in normal status.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactTahereh Rahiminia

Tehran University of Medical Sciences

t_rahiminia@razi.tums.ac.ir ; tahere_1980@yahoo.com+98 21 4490 4272

Outcome results

None listed

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