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The effect of different intratechal pethidine on shivering after caesarian surgery

The effect of different intratechal pethidine on shivering after caesarian surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138904101936N3
Enrollment
160
Registered
2010-10-15
Start date
2010-08-22
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 spinal anesthesia. --

Interventions

Intervention 1: Intratechal injection of 0.2 mg/kg pethidine plus lidocaine. Intervention 2: intratechal injection of lidocaine 100 mg two cc. Intervention 3: intratechal injection of 0.3 mg/kg of pet
Prevention
Intratechal injection of 0.2 mg/kg pethidine plus lidocaine
intratechal injection of lidocaine 100 mg two cc
intratechal injection of 0.3 mg/kg of pethidine plus lidocaine
Intratechal injection of 0.4 mg/kg pethidine plus lidocaine

Sponsors

Research committee of medical science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All women age between 15 and 50 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: 90 minute. Method of measurement: observation.

Secondary

MeasureTime frame
Post operative nausea and vomiting. Timepoint: 90 minute. Method of measurement: observation.;Hemodynamic change (BP Change). Timepoint: 90 minute. Method of measurement: NIBP monitoring.;Core temperature change. Timepoint: 90 minute. Method of measurement: core temperature monitoring.;Apgar score of neonate. Timepoint: In minute 5 and 10. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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