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The effect of intravenous meperdine vs intratechal meperdine on shivering during delivery under spinal anaesthesia

The effect of intravenous meperdine vs intratechal meperdine on shivering during delivery under spinal anaesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201301261936N11
Enrollment
78
Registered
2013-02-06
Start date
2013-02-05
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

Shivering after delivery. Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention 1: Control group received 12.5 mg bupivacaine 0.05, intratechaly plus 12.5 mg pethidine, intratechaly up to 3 cc. Intervention 2: Intervention group receive 12.5 mg bupivacaine 0.05, intr
Treatment - Drugs
Control group received 12.5 mg bupivacaine 0.05, intratechaly plus 12.5 mg pethidine, intratechaly up to 3 cc
Intervention group receive 12.5 mg bupivacaine 0.05, intratechaly plus 0.5 cc of normal saline up to 3 cc plus 12.5 mg pethidine, intravenously

Sponsors

Bushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: all women age between 15 and 45 years who are candidates for caesarean section and signed informed consent are eligible to join the study. Exclusion criteria: any contra indication for R/A and those who are sensitive to opioid.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post spinal shivering. Timepoint: 60 minute. Method of measurement: observation.

Secondary

MeasureTime frame
Post operative nausea and vomitting. Timepoint: 45 minute. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Abdolreza Najafianaraki

Bushehr University of Medical Sciences

dr.najafianaraki@gmail.com+98 77 1252 6801

Outcome results

None listed

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