Pethidine effect on feeding behavior and physiological parameters of the infant

The effect of Pethidine administration on feeding behavior and physiological parameters in newborns delivered by cesarean with spinal anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2017042233163N2

Enrollment

116

Registered

2017-08-14

Start date

2017-07-11

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

The effect of Pethidine administration on feeding behavior and physiological parameters in newborns delivered by cesarean with spinal anesthesia.

Interventions

Intervention 1: Intervention group: administration of 100 mg of pithidine intravenous infusion after the Cesaren section. Intervention 2: Control group: In this group was not given any narcotic drug.

Treatment - Drugs

Intervention group: administration of 100 mg of pithidine intravenous infusion after the Cesaren section

Control group: In this group was not given any narcotic drug. And non-opioid drugs such as diclofenac suppository is used to control pain.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria: mothers of childbearing age; The candidates are non-emergency cases; gestational age between 38 to 42 weeks; singleton pregnancy; tend to breastfeeding 6-ASA? (Anesthesia class specified by the Anesthesiologist); No history of mental illness and depression; Would like to participate in the study. Exclusion criteria: birth weight less than 2500 and more than 4,000 grams; First or fifth minute Apgar score less than seven; Meconium-stained amniotic fluid; Any abnormalities in the infant; using contraindicated drugs during breastfeeding; Formula feeding or bottle feeding; reluctant mother to continue to participate in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Feeding behavior. Timepoint: Three months after the start of the study. Method of measurement: Infant Breastfeeding Assessment Tool (IBAT).	—

Secondary

Measure	Time frame
Oxygen saturation. Timepoint: Three months after the start of the study. Method of measurement: Pulse oximeter.;Pulse rate. Timepoint: Three months after the start of the study. Method of measurement: Pulse oximeter.;Breathing. Timepoint: Three months after the start of the study. Method of measurement: Observation.;Body temperature. Timepoint: Three months after the start of the study. Method of measurement: Digital thermometer.	—

Measure

Time frame

Oxygen saturation. Timepoint: Three months after the start of the study. Method of measurement: Pulse oximeter.;Pulse rate. Timepoint: Three months after the start of the study. Method of measurement: Pulse oximeter.;Breathing. Timepoint: Three months after the start of the study. Method of measurement: Observation.;Body temperature. Timepoint: Three months after the start of the study. Method of measurement: Digital thermometer.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMontaseri Zohreh

Shiraz University of Medical Science, Shiraz Hazrate Fatemeh Nursing and Midwifery college

montaseriz@sums.ac.ir+98 71 3647 4255

Outcome results

None listed

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