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Ketamine vs Ephedrine on Post Spinal Hypotension in Caesarean Delivery

A

Ain Shams University

Status and phase

Completed
Phase 1

Conditions

Post Spinal Hypotension

Treatments

Drug: Ketalar
Drug: Ephedrine

Study type

Interventional

Funder types

Other

Identifiers

NCT07034911
FMASU MS130/2024

Details and patient eligibility

About

Comparing ketamine and ephedrine to decrease the incidence of post spinal hypotension after caesarean section delivery.

Full description

To compare the effect of ketamine versus ephedrine in decreasing the incidence of hypotension in caesarean section delivery a study group including 50 participants will receive ketamine and 50 group will receive ephedrine after the consent and detailed history the two groups will receive preload of 500ml enter acetate then dormicum for sedation then spinal anesthesia will be performed initial blood pressure and heart rate will be measured then every five minutes

Enrollment

100 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Patients undergoing Caesarian Section under spinal anesthesia,
  • Patients aged 18-45 years,
  • At term (≥37-week gestation),
  • American Society of Anaesthesiologists (ASA) physical status 1 or 2 Exclusion Criteria:
  • Pre-eclampsia,
  • Chronic hypertension, cardiovascular troubles,
  • Any contraindication to regional anesthesia such as local infection or bleeding disorders,
  • Any hypersensitivity to ketamine.
  • Declined informed consent.
  • American Society of Anaesthesiologists (ASA) physical status lll or lV

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

100 participants in 2 patient groups

Ketamine group
Active Comparator group
Description:
0.5mg/kg ketamine
Treatment:
Drug: Ketalar
Ephedrine group
Active Comparator group
Description:
15 mg ephedrine
Treatment:
Drug: Ephedrine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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