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Comparison the effectiveness of bupivacaine in spinal anesthesia with meperidine and sufentanil in patients undergoing elective cesarean section.

Comparison of the efficacy of bupivacaine in combination with sufentanil or bupivacaine in combination with meperidine or bupivacaine alone in spinal anesthesia in patients undergoing elective cesarean section

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191010045048N1
Enrollment
135
Registered
2019-10-18
Start date
2019-11-21
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Spinal anesthesia. Other complications of spinal and epidural anesthesia during pregnancy

Interventions

Intervention 1: Intervention group: In this group, 12.5 mg of bupivacaine, manufactured by Aboureihan pharmaceuticals, along with 20 mg of meperidine, manufactured by Caspian pharmaceuticals, were use

Sponsors

Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
17 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women 17 to 45 years of age Class of American Society of Anesthesiologists 1 as or 2

Exclusion criteria

Exclusion criteria: Patient dissatisfaction Coagulopathy Increased intracranial pressure Injection site infection Drastic decrease in intravascular volume Severe sensitivity to anesthetics and opioids Pregnancy hypertension Cesarean section requires blood transfusion Chronic itching Emergency cesarean section due to fetal distress Operation length greater than 1.5 hours

Design outcomes

Primary

MeasureTime frame
Time to reach the T10 anesthesia. Timepoint: During surgery. Method of measurement: Physical examination.;The time to reach the highest level of Dermatome anesthesia. Timepoint: During surgery. Method of measurement: Physical examination.;Anesthesia down to T10 level. Timepoint: During surgery. Method of measurement: Physical examination.;Time to reach full block. Timepoint: After surgery. Method of measurement: Physical examination.;Motor recovery time. Timepoint: After surgery. Method of measurement: Physical examination.;Postoperative drowsiness. Timepoint: After surgery. Method of measurement: Physical examination.;Amount of Diclofenac consumption. Timepoint: After surgery. Method of measurement: check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Noruzi

Zahedan University of Medical Sciences

dr.nnorouzi@zaums.ac.ir+98 54 3329 5564

Outcome results

None listed

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