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Comparison of Fractionated Versus Bolus Administration of Different Doses of Hyperbaric Bupivacaine Combined With Opioids in Spinal Anesthesia for Caesarean Section

B

Bogomolets National Medical University

Status

Completed

Conditions

Spinal Anesthesia for Cesarean Section

Treatments

Procedure: Fractionated anesthesia
Procedure: Bolus anesthesia

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study aimed to compare the effectiveness and safety of fractionated versus bolus administration of different doses of hyperbaric bupivacaine (0.06 and 0.07 mg/cm height) combined with opioids in spinal anesthesia for cesarean section, with detailed evaluation of maternal hemodynamic effects, block characteristics and side effects.

Enrollment

99 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • singleton full-term pregnancy scheduled for cesarean section under spinal anesthesia
  • ASA physical status II-III
  • age 18-50 years
  • height from 140 to 180 cm
  • body weight from 40 to 130 kg

Exclusion criteria

  • patient refusal
  • contraindications to spinal anesthesia
  • allergy to amide-type local anesthetics

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

99 participants in 3 patient groups

Bolus bupivacaine (0.07 mg/cm)
Active Comparator group
Treatment:
Procedure: Bolus anesthesia
Fractionated bupivacaine (0.07 mg/cm)
Experimental group
Treatment:
Procedure: Fractionated anesthesia
Fractionated bupivacaine (0.06 mg/cm)
Active Comparator group
Treatment:
Procedure: Fractionated anesthesia

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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