? Comparing dexmedmotidine and remifentanil to reduce pain in disc

? Comparing dexmedmotidine and remifentanil to reduce pain in disc hernia

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20141209020258N108

Enrollment

Registered

2019-04-27

Start date

2018-12-22

Completion date

Unknown

Last updated

2019-05-21

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

Conditions

Disc herniation. Traumatic rupture of lumbar intervertebral disc, sequela

Interventions

Intervention 1: Intervention group1: Acetaminophen 2 grams and 0.15 micrograms (mcg) per kilogram (kg) of body weight per hour Dexmedmotidine pumped .The volume of material is diluted to 100 millilit

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Both gender ASA class 1 and 2 Candidate surgery of hernia disc No allergy to drug use No addiction

Exclusion criteria

Exclusion criteria: Dissatisfaction Allergy to drug use

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: Recovery, 2 and 4 and 6 and 12 hours after surgery. Method of measurement: Visual analog scale.;Relaxation. Timepoint: 24 hours after surgery. Method of measurement: Ramsy score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Alireza Kamali

Arak University of Medical Sciences

alikamaliir@yahoo.com+98 86 3222 2003

Outcome results

None listed

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