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Efficacy of Dexamethasone in Attenuation of Postinduction Hypotension in Geriatric Patients Undergoing General Anesthesia

A

Ain Shams University

Status and phase

Completed
Phase 4

Conditions

Hypotension

Treatments

Drug: Dexamethasone
Other: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT04908592
FMASU MS 289/ 2021

Details and patient eligibility

About

  • Geriatric patients who undergo general anesthesia experience post induction hypotension which is treated with intravenous fluids and ephedrine. The main cause of post-induction hypotension is the decrease in the sympathetic outflow causing arterial vasodilatation, a decrease in venous return and consequently the activation of the Bezold Jarish reflex (BJR) that elicits a triad of bradycardia, vasodilatation and further hypotension. BJR is elicited by activation of 5-HT3 receptors within the intracardiac vagal nerve endings.
  • Glucocorticoids in general inhibit 5-HT3 expression and dexamethasone was found to decrease the level of 5-HT3 in the cerebral cortex and hippocampus in developing rats. So, the research team hypothesizes that dexamethasone can attenuate the postinduction hypotension in geriatric patients undergoing general anesthesia if administered preoperatively.

Enrollment

100 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. American Society of Anesthesiologists (ASA) Physical Status Class-I and II.
  2. Elective surgery under general anesthesia.

Exclusion criteria

  1. Emergency surgeries.
  2. Ischemic heart disease.
  3. Peptic ulcer & active infection.
  4. Psychiatric disorder.
  5. Patients on steroids or serotonin related medications (e.g., selective serotonin reuptake inhibitor).

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 2 patient groups, including a placebo group

D Group (50 patients)
Active Comparator group
Treatment:
Drug: Dexamethasone
C Group (50 patients)
Placebo Comparator group
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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