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A Comparison of the effects of 5% lidocaine and 5% meperidine plus 5% lidocaine on hypotension and duration of analgesia postoperative in cesarean section for spinal anesthesia

A Comparison of the effects of 5% lidocaine and 5% meperidine plus 5% lidocaine on hypotension and duration of analgesia postoperative for cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201108286808N3
Enrollment
50
Registered
2012-06-02
Start date
2008-09-05
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

non-emergency caesarean. Delivery by elective caesarean section

Interventions

Intervention 1: Intervention group: injection 5%meperidine1.25 mg/kg and 5% heavy lidocaine 60-75 mg for spinal anesthesia. Intervention 2: Control group: injection 5% heavy lidocaine alone60-75 mg
Treatment - Drugs
Intervention group: injection 5%meperidine1.25 mg/kg and 5% heavy lidocaine 60-75 mg for spinal anesthesia
Control group: injection 5% heavy lidocaine alone60-75 mg for spinal anesthesia

Sponsors

Zahedan University of Medical Scienses
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria : Elective cesarean, previous cesarean, dystocia , full term pregnant women. Exclusion criteria: emergency cesarean, Preterm delivery.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Duration of post operative analgesia. Timepoint: Upon the occurrence of pain after surgery. Method of measurement: Pain recorded in form the precisely.;Hypotention. Timepoint: Prior to spinal anesthesia - Every 5 minutes during surgery until the end of surgery. Method of measurement: The mercury manometer.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Tolyat

Birjand University of Medical Sciences

tolyatm@yahoo.com+98 56 1444 9056

Outcome results

None listed

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