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Effects of Intrathecal Midazolam (1mg) With Hyperbaric Bupivacaine 0.5% (15mg) for Spinal Anesthesia for C-section

S

Superior University

Status

Active, not recruiting

Conditions

Cesarean Section Complications

Treatments

Diagnostic Test: group 1

Study type

Observational

Funder types

Other

Identifiers

NCT06748794
MSAHS/Batch-Spring23/049

Details and patient eligibility

About

This study evaluates the effects of intrathecal midazolam (1 mg) combined with hyperbaric bupivacaine 0.5% (15 mg) for spinal anesthesia in cesarean section patients.

Full description

The addition of midazolam, a benzodiazepine with analgesic and anxiolytic properties to bupivacaine is hypothesized to enhance the quality of anesthesia and postoperative pain relief without significant side effects. A comparative analysis was conducted to assess sensory and motor block characteristics, postoperative analgesia duration, maternal hemodynamic stability, and neonatal outcomes.

Enrollment

64 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Female patients presented for elective cesarean section.
  • All ASA I & II patients .
  • Age between 18 to 35 years.

Exclusion criteria

  • Contraindication to spinal anesthesia.
  • Patient not willing or previous bad experience with it.
  • All ASA III & IV class was excluded from the study.
  • Patients with documented bleeding disorders i.e. low platelet count, deranged PT/APTT/INR, DIC etc.
  • Hypertensive patients
  • Patients with Diabetes mellitus.
  • Obese patients BMI >30.
  • PIH (pre- eclampsia and eclapmsia)"

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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