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Effect of Intraoperative IV Ketamine on Postoperative Morphine Consumption During Intestinal Surgery

A

Assiut University

Status

Unknown

Conditions

Postoperative Analgesia

Treatments

Drug: Ketamine Hydrochloride
Drug: Normal saline

Study type

Interventional

Funder types

Other

Identifiers

NCT03344393
17200147

Details and patient eligibility

About

.The aim of this study is to identify the analgesic effect of intraoperative ketamine intravenous infusion on patients undergoing intestinal surgery and its effect on salivary cortisol and alpha amylase levels as indicator of its effect.

Full description

I- Group K (ketamine): 30 patients will receive intraoperative intravenous ketamine infusion.

II- Group C (control): 30 patients will receive intraoperative intravenous normal saline infusion.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    • Patient's status ASA status-I and II.
  • Patients age above 18 years old.
  • Patients scheduled for intestinal surgery.

Exclusion criteria

  • Patient refusal.
  • Patients with known allergy to ketamine or morphine.
  • Patients with significant hepatic dysfunction.
  • Patients with severe renal disease.
  • Significant Heart disease.
  • Patients with chronic pain.
  • Regular use analgesics, antidepressants or opioids in last 2 months.
  • Any known convulsive disorder.
  • Morbid obesity (BMI>35).
  • Patients with autoimmune disease
  • Patients on corticosteroid therapy
  • Pregnancy.
  • Breast feeding.
  • Woman under hormonal treatment.
  • Oral disease.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

ketamine hydrochloride
Active Comparator group
Description:
intravenous ketamine infusion in the intraoperative period
Treatment:
Drug: Ketamine Hydrochloride
normal saline
Active Comparator group
Description:
intravenous normal saline infusion in the intraoperative period
Treatment:
Drug: Normal saline

Trial contacts and locations

0

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Central trial contact

mohamed aly, MD

Data sourced from clinicaltrials.gov

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