Evaluation of effect ketamine infusion in acute post operative pain control

Evaluation of effect ketamine infusion in perioperative posterior spine fixation surgery in acute post operative pain control

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20161220031487N11

Enrollment

Registered

2024-09-10

Start date

2024-09-22

Completion date

Unknown

Last updated

2024-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain. Acute pain, not elsewhere classified

Interventions

Intervention 1: Intervention group: In order to investigate and manage pain after surgery, patients in this group undergo ketamine infusion during surgery. During the procedure, ketamine with a concen

Eligibility

Sex/Gender

All

Age

14 Years to 70 Years

Inclusion criteria

Inclusion criteria: A person with normal health A person with a mild systemic disease,

Exclusion criteria

Exclusion criteria: Emergency patients History of allergy to any of the drugs used in the project Body mass index greater than 35 Seizures Ischemic heart disease Addiction to opioids Repeated spine surgery

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 0, 2, 6 and 12 hours after surgery. Method of measurement: Based on a numerical rating scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Sarami

Iran University of Medical Sciences

Vahidsarami128@gmail.com0098 21 64351

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026