success rate in mothers under painless delivery by epidural anesthesia

Comparison of breastfeeding success rate in mothers under painless delivery by epidural anesthesia with normal vaginal delivery

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160103025821N7

Enrollment

150

Registered

2019-06-13

Start date

2019-06-20

Completion date

Unknown

Last updated

2019-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lactation success rate.

Interventions

Intervention 1: The intervention group included women with epidural method, receiving bupivacaine 0.12% 125/0% or rupivacaine 0.1-0.2% + fentanyl 51 µg per 10-15 ml volume. Intervention 2: Control gro

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: single baby nollipar woman, Pregnancy up to 37 weeks; Demand for labor with epidural; Healthy baby

Exclusion criteria

Exclusion criteria: multi-parity; no willing to lactation, Embryonic anomalies or metabolic diseases that make it impossible to breastfeed; no willing to lactation, insatis fact for epidural anesthesia APGAR score less than 7; Asafixy baby

Design outcomes

Primary

Measure	Time frame
Respiratory depression. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: PHysical examination.;Hypotension. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: Monitoring, Sphygmomanometer tool.;Backpain. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: History.	—

Measure

Time frame

Respiratory depression. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: PHysical examination.;Hypotension. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: Monitoring, Sphygmomanometer tool.;Backpain. Timepoint: Immediately after the intervention, after 5 minute, after 10 minute, after 20 minute, after 40 minute, after 60 minute, after 1.5 hour, after 2 hour, after 3 hour, . Method of measurement: History.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hojjat Pourfathi

Tabriz University of Medical Sciences

pourfathih@tbzmed.ac.ir+98 914 313 8969

Outcome results

None listed

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