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Comparison of frequency of cesarean section and the average of delivery ?phases between Epidural analgesia versus no analgesia in labor

Comparison of frequency of cesarean section and the average of delivery ?phases between Epidural analgesia versus no analgesia in labor

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017102420258N63
Enrollment
120
Registered
2017-11-16
Start date
2017-06-05
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. Single spontaneous delivery

Interventions

Intervention 1: Intervention group: Women will done delivery with epidural anesthesia (4-6 milliliter ?Marcain 0/125 percent and single dose 5 micro gram Fentanyl and preservative dose ?Marcain 0/12
Treatment - Drugs
Intervention group: Women will done delivery with epidural anesthesia (4-6 milliliter ?Marcain 0/125 percent and single dose 5 micro gram Fentanyl and preservative dose ?Marcain 0/125 percent and 0/
Control group: Delivery is performed without analgesia.

Sponsors

Vice chancellor for research, Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant woman; single fetus; pregnant women candidates vaginal delivery; pregnant women candidates epidural; nuliparous; ASA class I and II; 37 to 42 weeks Exclusion criteria: Mothers with more than one fetus; multiparty mothers; patients referring to urgency; Patients with topical anesthetics and narcotic; block placenta infection; failure in epidural anesthesia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence cesarean ?. Timepoint: after delivery. Method of measurement: mount.;Mean of time of delivery phases. Timepoint: after delivery. Method of measurement: Minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Maryam Shokrpour

Arak University of Medical Sciences

m.shokrpour@yahoo.com+98 86 3222 2003

Outcome results

None listed

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