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Side effects of entonox on mother & new born

Determination of side effects of entonox on mother & new born in primiparus pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201012035299N1
Enrollment
178
Registered
2011-11-04
Start date
2011-01-13
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

delivery related complications. Excessive intrapartum haemorrhage

Interventions

Intervention 1: In the case group entonox was administrated in active phase of labor & the patient inspirited in the mask 30 seconds before beginning of labor pain. Intervention 2: In the control gro
Treatment - Drugs
In the case group entonox was administrated in active phase of labor & the patient inspirited in the mask 30 seconds before beginning of labor pain.
In the control group oxygen was administrated in active phase of labor.

Sponsors

Hamadan's Fatemieh Hospital delivery ward
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria :primiparus;term pregnancy(37-42wks);active phase of labor(cervical dilatation of 3-4 cm);no medical disease or obstetrical complication in mother & fetus Exclusion criteria :women who refuse to participate in this study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Placental abruption. Timepoint: during intervention. Method of measurement: observation.;Accelerated labor. Timepoint: during intervention. Method of measurement: observation.;Neonatal APGAR score minute 1&5. Timepoint: 1&5 minutes after delivery. Method of measurement: observation.;Final route of delivery. Timepoint: during intervention. Method of measurement: observation.;Fetal meconium passing. Timepoint: during intervention. Method of measurement: observation.;Maternal complications. Timepoint: 6 hours after delivery. Method of measurement: question sheet.;Used pads. Timepoint: 6 hours after itervention. Method of measurement: question sheet.;Hb. Timepoint: Before & 6 hours after intervention. Method of measurement: grams per desiliteres.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shala Nasrolahi

Hamedan University of Medical Sciences

sh_nasrolahi@yahoo.com+98 81 1827 6295

Outcome results

None listed

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