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Evaluation the effect of dexamethazone and promethazin with meperidin in rate of labor pain and duration of labor in women with normal vaginal delivery

Comparison the effect of dexamethazone and promethazin with meperidin in rate of nausea and vomiting, labor pain and duration of labor in women with normal vaginal delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201406021951N4
Enrollment
60
Registered
2014-09-17
Start date
2013-04-21
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

Normal vaginal delivery. Single live birth

Interventions

Intervention 1: Intervention1:100 mg meperidin with 2cc normal saline/ IM and 8 mgr dexamethazone/IV will injected. Intervention 2: Intervention 2:100mg meperidin with 50 mgr promethazin/IM and 2 cc n
Treatment - Drugs
Intervention1:100 mg meperidin with 2cc normal saline/ IM and 8 mgr dexamethazone/IV will injected.
Intervention 2:100mg meperidin with 50 mgr promethazin/IM and 2 cc normal saline/IV will injected.

Sponsors

Tehran University of Medical Sciences, Deputy of Research
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
74 Years to 52 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: singleton pregnancy with cephalic presentation, gestational age 38 to 42 weeks with an uncomplicated vaginal delivery. Exclusion criteria: mother's weight less than 50 kg or more than 100 kg, use of epidural anesthesia, drug and alcohol abuse, history of allergy to drugs used in the study and pre-eclampsia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of labor pain. Timepoint: Before intervention and 30,60,90 and 120 min after intervention. Method of measurement: Visual scale.;Duration of labor. Timepoint: Before intervention and 30,60,90 and 120 min after intervention. Method of measurement: Timer.;The Rate of nausea and vomiting. Timepoint: Before intervention and 30,60,90 and 120 min after intervention. Method of measurement: Questionnaire.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Nasrin Faridi Tazeh-kand

Arash Women 's Hospital, Tehran University of Medical Sciences

nfaridi@sina.tums.ac.ir+98 21 7771 9922

Outcome results

None listed

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